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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789780Generated: October 30, 2026

2-(difluoromethyl)-1H-1,3-benzodiazole → 2-(6-Amino-2-difluoromethylbenzimidazol-1-yl)-4,6-dimorpholinopyrimidine

https://huagongshe.com/reaction/1789780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(difluoromethyl)-1H-1,3-benzodiazoleHCID 597703—
Reactant2-(2-Difluoromethyl-6-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidineHCID 22036868—
Reactant2-(2-Difluoromethyl-5-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidineHCID 22036886—
Product2-(6-Amino-2-difluoromethylbenzimidazol-1-yl)-4,6-dimorpholinopyrimidineHCID 2203689988%

Reaction Steps

In accordance with the procedure of the Example 1 except that 2-difluoromethylbenzimidazole in (1) of the Example 1 was replaced by 2-difluoro-6-nitrobenzimidazole, a mixture of 2-(2-difluoromethyl-5-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine with 2-(2-difluoromethyl-6-nitrobenzimidazol-1-yl)-4,6-dimorpholinopyrimidine was obtained. In accordance with the procedure of (3) of the Example 8, using 0.92 g (2.0 mmol) of this mixture, 0.76 g (yield: 88%) of the titled compound was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071189B2
Source datasetuspto-grants-2006_07
ORD IDord-ded3e55de6ba4c58b7ab83aa957d0d54
Source noteuspto-grants-2006_07