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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460707Generated: October 30, 2026

N-bromobutanimide → HCID 58825057, compound

https://huagongshe.com/reaction/460707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 15957952HCID 15957952—
SolventDichloromethaneHCID 6344—
ProductHCID 58825057HCID 5882505711.9%

Reaction Steps

To an ice cold solution of 50 mg (0.113 mmol) of 6-(4-benzyloxy-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid methyl ester in 2 mL of dichloromethane (DCM) was added a solution of 21 mg (0.118 mmol) of N-bromosuccinimide (NBS) in 1 mL of DCM and the resulting mixture was allowed to warm up to rt and stirred at rt overnight. The reaction mixture was concentrated to give a residue which was chromatographed on silica gel (5% ethyl acetate in dichloromethane) to afford 7 mg (11% yield) of 6-(4-benzyloxy-phenyl)-3-bromo-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid methyl ester as a colorless oil as indicated by 1H NMR (90% purity); LC-MS—calcd for C27H26BrN3O3 [M++H]+: 520.12, found: 520.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196111B2
Source datasetuspto-grants-2007_03
ORD IDord-8fcab269901a484c96a194bd0fabbbc4
Source noteuspto-grants-2007_03