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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729539Generated: October 29, 2026

Chloroform → HCID 68908188, compound

https://huagongshe.com/reaction/729539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 11361492HCID 11361492—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductHCID 68908188HCID 68908188—

Reaction Steps

The title compound was analogously synthesized by the method described in Example 55 with the addition of one step. To a solution of benzyl-(4-[5-(2,5-diaza-bicyclo[2.2.1]hept-2-yl)imidazo[1,2-c]pyrimidin-7-yl]pyridin-2-yl)amine (0.400 g) was added chloroform (4 mL) followed by acetone (5 mL), and sodium triacetoxy borohydride (0.600 mg) at 70° C. After 30 min, work up between dichloromethane and sodium bicarbonate followed by flash column purification afforded the title compound as an off white solid. MS (ES+): 440 (M+H)+; (ES−): 438(M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582631B2
Source datasetuspto-grants-2009_09
ORD IDord-1d467775dee842fc9a095aa5403c23e9
Source noteuspto-grants-2009_09