# US 12,180,201 B1 · 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide as an antimicrobial compound

> Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt

- Number: US 12,180,201 B1
- Document ID: US12180201B1
- Status: Granted
- Kind: B1
- Application number: 18/429,757
- Filed: 2024-02-01
- Granted: 2024-12-31
- Earliest claimed: 2023-10-23
- Assignees: King Faisal University
- Applicants: King Faisal University
- Inventors: Hany Mohamed Abd El-Lateef Ahmed; Mai Mostafa Khalaf Ali; Antar Ahmed Abdelhamid Ahmed; Amer A. Amer
- Web page: https://patentgrep.com/patent/US12180201B1

## CPC

- C07D 413/12: linked by a chain containing hetero atoms as chain links
- A61P 31/04: Antibacterial agents
- A61P 31/10: Antimycotics
- C07D 413/14: containing three or more hetero rings
- C07D: HETEROCYCLIC COMPOUNDS (macromolecular compounds C08)
- A61P: SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

## Abstract

A 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound, its synthesis, and its use as an antimicrobial agent.

## Claims

### Claim 1

A method of making 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide, the method comprising:
adding carbonyldiimidazole (CDI) to a mixture of isonicotinic acid in acetonitrile to obtain a first reaction mixture;
stirring the first reaction mixture;
adding (1,3-benzoxazol-2-yl) acetonitrile to the first reaction mixture to obtain a second reaction mixture;
stirring the second reaction mixture;
purifying a formed precipitate by filtering and recrystallization using acetonitrile; and
obtaining 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide having the structure:

### Claim 2 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein stirring the first reaction mixture lasts for at least about 35 minutes.

### Claim 3 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the first reaction mixture is stirred at room temperature.

### Claim 4 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the second reaction mixture is stirred for at least about 4 hours.

### Claim 5 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the formed precipitate is washed with cold acetonitrile.

### Claim 6 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the isonicotinic acid and CDI are added in about a 2:2.4 molar ratio.

### Claim 7 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the isonicotinic acid, CDI, and (1,3-benzoxazol-2-yl) acetonitrile are added in about a 2:2.4:2 molar ratio.

### Claim 8 (depends on 1)

The method of making the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound of claim 1, wherein the 2-(benzo[d]oxazol-2-yl)-N′-(isonicotinoyloxy)acetimidamide compound is obtained in a yield of about 88%.
