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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717849Generated: October 30, 2026

Boron tribromide → HCID 178463543, compound

https://huagongshe.com/reaction/717849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 178496657HCID 178496657—
SolventDichloromethaneHCID 6344—
ProductHCID 178463543HCID 17846354311%

Reaction Steps

To a cooled solution of N-(1-{8-chloro-5-[(3R)-3-methoxypyrrolidin-1-yl]imidazo[1,5-a]pyridin-6-yl}ethyl)-9H-purin-6-amine (27.0 mg, 0.0654 mmol) in methylene chloride (1.0 mL) at −78° C. under an atmosphere of nitrogen was added slowly 1.0 M boron tribromide in methylene chloride (0.47 mL, 0.47 mmol). The mixture was allowed to warm up to room temperature and stirred for 30 minutes. The resultant mixture was quenched with Na2CO3 (aq). The cloudy suspension was filtered and washed with water. The filtrate was extracted with ethyl acetate and the organic layer was washed with brine and evaporated. Purification by preparative LCMS (pH 10) gave the desired compound (2.8 mg, 11%). LCMS calculated for C18H20ClN8O (M+H)+: m/z=399.1. found: 398.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193721B2
Source datasetuspto-grants-2015_11
ORD IDord-864d70838b2d4436804081c0b9c39bb2
Source noteuspto-grants-2015_11