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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470332Generated: October 30, 2026

Methyl 2,2,2-trichloroacetimidate → HCID 178494095, compound

https://huagongshe.com/reaction/470332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2,2,2-trichloroacetimidateHCID 100479—
ReactantHCID 59784760HCID 59784760—
SolventAcetic AcidHCID 176—
ProductHCID 178494095HCID 178494095—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-amino-4-(2-methoxypyridin-3-yl)phenylamine 3 obtained from above reaction (0.215 g, 1 mmol) in acetic acid (2 mL) cooled to 0° C. was added methyl trichloroacetimidate (0.193 g, 1.1 mmol) under N2 atmosphere and resulting reaction mixture was stirred at room temperature for 3 h. Acetic acid was evaporated to give crude 5-(2-methoxypyridin-3-yl)-2-(trichloromethyl)-1H-benzimidazole which was used as such in the following step (0.3 g). Reference: Louvet, P.; Lallement, G.; Pemot-Marino, I.; Luu-Duc, C.; Blanchet, G. Eur. J. Med. Chem. 1993, 28, 71-75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629147B2
Source datasetuspto-grants-2014_01
ORD IDord-60dd7c9d903f413c95d6fc238a2188bf
Source noteuspto-grants-2014_01