Methyl 2,2,2-trichloroacetimidate → HCID 178497591, compound

HRID 18611Notes

Reaction equation

HRID 18611 reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([CH3:10])[C:7]([NH2:11])=[C:6]([NH2:12])[CH:5]=1.CO[C:16](=[NH:21])[C:17]([Cl:20])([Cl:19])[Cl:18]>>[CH3:1][O:2][C:3]([C:4]1[CH:9]=[C:8]([CH3:10])[C:7]2[NH:11][C:16]([C:17]([Cl:20])([Cl:19])[Cl:18])=[N:12][C:6]=2[CH:5]=1)=[O:13].[CH3:1][O:2][C:3]([C:4]1[CH:9]=[C:8]([CH3:10])[C:7]2[NH:11][C:16]([C:17]([Cl:18])([Cl:19])[Cl:20])=[N:21][C:6]=2[CH:5]=1)=[O:13]

Participants

3

Procedure

7-Methyl-2-trichloromethyl-1H-benzoimidazole-5-carboxylic acid methyl ester 7-Methyl-2-trichloromethyl-1H-benzoimidazole-5-carboxylic acid methyl ester was prepared by a procedure according to example 5 (i) starting from 404.0 mg (2.20 mmol) 3,4-Diamino-5-methyl-benzoic acid methyl ester and 0.39 mL (3.08 mmol) 2,2,2-trichloro-acetimidic acid methyl ester.

Sources & evidence

ORD record
ord-7ad6cc8a6a854e76b8d70c93dbd50135
Source dataset
uspto-grants-2010_06
Patent number
US07741341B2

Reaction notes

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