Method for producing bicyclic compound
AssigneeOno Pharmaceutical Co., Ltd.
InventorsHideki Moriguchi, Yusuke Tanaka, Tatsunori Ino, Tohru Kambe, Taihei Nishiyama, Shinichiro Tsujiyama, Yohei Ueda
Life of this patent
Estimating the term…
Abstract
A method for producing a compound, such as 2-propanyl 4-{(3S,5aR,6R,7R,8aS)-6-[(1E,3R)-4-(2,5-difluorophenoxy)-3-hydroxy-1-buten-1-yl]-7-hydroxyoctahydro-2H-cyclopenta[b]oxepin-3-yl}butanoate, and a novel intermediate suitable for the method, whereby the compound can be stably supplied with a high total reaction yield, by changing the starting material and improving the metathesis reaction, asymmetric reduction reaction and the like.
Claims5
A method for producing a compound represented by formula (G) or a salt thereof:
- wherein, R1 represents a C1-6 alkyl group optionally substituted with a hydroxyl group or a C1-4 alkoxy group, Z represents (1) —(CH2)m—, (2) —(CH2)n—CH═CH—, or (3) —(CH2)p-A-CH2—, A represents an oxygen atom, or a sulfur atom, m represents an integer of 1 to 6, n represents an integer of 1 to 4, and p represents an integer of 1 to 4, and T1 represents (1) a p-phenybenzoyl group, (2) a methyl group, (3) a trityl group, (4) a methoxymethyl group, (5) a 1-ethoxyethyl group, (6) a methoxyethoxymethyl group, (7) a benzyloxymethyl group, (8) a trimethylsilyl group, (9) a triethylsilyl group, (10) a t-butyldimethylsilyl group, (11) a t-butyldiphenylsilyl group, (12) a triisopropylsilyl group, (13) a benzyl group, (14) a p-methoxybenzyl group, (15) an acetyl group, (16) a pivaloyl group, (17) a benzoyl group, (18) an allyloxycarbonyl group, (19) a 2,2,2-trichloroethoxycarbonyl group, (20) a t-butoxycarbonyl group, (21) an allyl group, or (22) a tosyl group,
- the method comprising the following steps (i) to (vi):
- step (i):
- subjecting a compound represented by formula (A):
- wherein, T2 represents a benzyl group, and other symbols represent the same meanings as those described above,
- to a reduction reaction to produce a compound represented by formula (B):
- wherein, all symbols represent the same meanings as those described above,
- or a salt thereof;
- step (ii):
- subjecting the compound represented by formula (B) obtained in the step (i) or a salt thereof to a reaction in an organic solvent, in the presence of a base using a Wittig reagent to produce a compound represented by formula (C):
- wherein, all symbols represent the same meanings as those described above,
- or a salt thereof;
- step (iii):
- subjecting the compound represented by the formula (C) obtained in the step (ii) or a salt thereof and a compound represented by formula (a):
- wherein, X represents a halogen atom, a tosyloxy (TsO) group, or a mesyloxy (MsO) group, and other symbols represent the same meanings as those described above,
- to an alkylation reaction to produce a compound represented by formula (D):
- wherein, all symbols represent the same meanings as those described above;
- step (iv):
- subjecting the compound represented by the formula (D) obtained in the step (iii) to a metathesis reaction to produce a compound represented by formula (E):
- wherein, all symbols represent the same meanings as those described above;
- step (v):
- subjecting the compound represented by the formula (E) obtained in the step (iv) to an asymmetric reduction reaction to produce a compound represented by formula (F):
- wherein, all symbols represent the same meanings as those described above;
- and
- step (vi):
- subjecting the compound represented by the formula (F) obtained in the step (v) to a deprotection reaction to produce the compound represented by the formula (G) or a salt thereof.
A method for producing a compound represented by formula (K):
- wherein, Y represents —CH2—, —O— or —S—, represents a C3-10 carbocycle or a 3- to 10-membered heterocycle optionally substituted with 1 to 5 substituents selected from the group consisting of (1) a halogen atom, (2) CF3, (3) OCF3, (4) a C1-4 alkoxy group, (5) a C1-4 alkyl group, (6) a hydroxyl group, and (7) a nitrile group, R1 represents a C1-6 alkyl group optionally substituted with a hydroxyl group or a C1-4 alkoxy group, Z represents (1) —(CH2)m—, (2) —(CH2)n—CH═CH—, or (3) —(CH2)p-A-CH2—, A represents an oxygen atom, or a sulfur atom, m represents an integer of 1 to 6, n represents an integer of 1 to 4, and p represents an integer of 1 to 4,
- the method comprising:
- producing a compound represented by formula (G) or a salt thereof from a compound represented by formula (A) according to steps (i) to (vi):
- wherein, T1 represents (1) a p-phenybenzoyl group, (2) a methyl group, (3) a trityl group, (4) a methoxymethyl group, (5) a 1-ethoxyethyl group, (6) a methoxyethoxymethyl group, (7) a benzyloxymethyl group, (8) a trimethylsilyl group, (9) a triethylsilyl group, (10) a t-butyldimethylsilyl group, (11) a t-butyldiphenylsilyl group, (12) a triisopropylsilyl group, (13) a benzyl group, (14) a p-methoxybenzyl group, (15) an acetyl group, (16) a pivaloyl group, (17) a benzoyl group, (18) an allyloxycarbonyl group, (19) a 2,2,2-trichloroethoxycarbonyl group, (20) a t-butoxycarbonyl group, (21) an allyl group, or (22) a tosyl group, and other symbols represent the same meanings as those described above,
- step (i):
- subjecting a compound represented by formula (A):
- wherein, T2 represents a benzyl group, and other symbols represent the same meanings as those described above,
- to a reduction reaction to produce a compound represented by formula (B):
- wherein, all symbols represent the same meanings as those described above,
- or a salt thereof;
- step (ii):
- subjecting the compound represented by formula (B) obtained in the step (i) or a salt thereof to a reaction in an organic solvent, in the presence of a base using a Wittig reagent to produce a compound represented by formula (C):
- wherein, all symbols represent the same meanings as those described above,
- or a salt thereof;
- step (iii):
- subjecting the compound represented by the formula (C) obtained in the step (ii) or a salt thereof and a compound represented by formula (a):
- wherein, X represents a halogen atom, a tosyloxy (Ts0) group, or a mesyloxy (Ms0) group, and other symbols represent the same meanings as those described above,
- to an alkylation reaction to produce a compound represented by formula (D):
- wherein, all symbols represent the same meanings as those described above;
- step (iv):
- subjecting the compound represented by the formula (D) obtained in the step (iii) to a metathesis reaction to produce a compound represented by formula (E):
- wherein, all symbols represent the same meanings as those described above;
- step (v):
- subjecting the compound represented by the formula (E) obtained in the step (iv) to an asymmetric reduction reaction to produce a compound represented by formula (F):
- wherein, all symbols represent the same meanings as those described above;
- and
- step (vi):
- subjecting the compound represented by the formula (F) obtained in the step (v) to a deprotection reaction to produce the compound represented by the formula (G) or a salt thereof;
- producing a compound represented by formula (I) or a salt thereof from the compound represented by the formula (G) or a salt thereof according to steps (vii) to (viii):
- wherein, all symbols represent the same meanings as those described above,
- step (vii):
- subjecting a compound represented by formula (G):
- wherein, all symbols represent the same meanings as those described above, or a salt thereof to an oxidation reaction to produce a compound represented by formula (H):
- wherein, all symbols represent the same meanings as those described above;
- and
- step (viii):
- subjecting the compound represented by the formula (H) obtained in the step (vii) and a compound represented by formula (b):
- wherein, R101 represents a C1-6 alkyl group, and other symbols represent the same meanings as those described above,
- to a reaction in an organic solvent, in water, or in a mixed solution thereof, in the presence of a base, in the presence or absence of an additive to produce the compound represented by the formula (I) or a salt thereof;
- and
- producing the compound represented by the formula (K) according to steps (ix) to (x):
- step (ix):
- subjecting a compound represented by formula (I):
- wherein, all symbols represent the same meanings as those described above, or a salt thereof, to an asymmetric reduction reaction to produce a compound represented by formula (J) or a salt thereof:
- wherein all symbols represent the same meanings as those described above;
- and
- step (x):
- subjecting the compound represented by the formula (J) or a salt thereof to a deprotection reaction to produce the compound represented by the formula (K).
Dependencies are inferred from the claim text.