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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099752Generated: October 30, 2026

Benzyl Bromide → HCID 178436411, compound

https://huagongshe.com/reaction/2099752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 178436413HCID 178436413—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 178436411HCID 178436411—

Reaction Steps

A mixture of 4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidine-1-carboxylic acid [2-(7-ethyl-3-methyl-1H-indazol-5-yl)-1-(1H-tetrazol-5-yl)-ethyl]-amide (30 mg, 0.05 mmol, 1.0 equiv), sodium carbonate (18.0 mg, 3.0 equiv), and benzyl bromide (8 μL, 1.1 equiv) were combined in dimethylsulfoxide and the mixture stirred at room temperature overnight. The mixture was then diluted with water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water (3×), brine (3×), dried over sodium sulfate, and concentrated. Purification by preparative HPLC afforded a mixture of the two alkylated regioisomers which were not separated. LC/MS: tR=1.68 min, 619.44 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-378a70bab0cb45d4951e129d0d8ac706
Source noteuspto-grants-2009_08