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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099779Generated: October 30, 2026

Benzyl Bromide → HCID 57794685, compound

https://huagongshe.com/reaction/2099779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 11409395HCID 11409395—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57794685HCID 57794685—

Reaction Steps

N-(1-(1H-Imidazol-2-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl)-4-(2-oxo-1,2-dihydroquinazolin-3(4H)-yl)piperidine-1-carboxamide (100 mg, 0.2 mmol) and benzyl bromide (25.0 μL, 1.1 equiv) were combined in dimethyl sulfoxide (0.6 mL). After stirring at room temperature for 16 h, the reaction mixture was poured into ice water and extracted with ethyl acetate (2×). The organic layer was washed with brine (2×), dried over sodium sulfate, concentrated, and purified by column chromatography to afford 14.0 mg (12%). 1H-NMR (CD3OD, 500 MHz) δ 1.58-1.70 (m, 4H), 2.48 (s, 3H), 2.75-2.84 (m, 2H), 3.36-3.43 (m, 2H), 4.02-4.14 (m, 3H), 4.23 (s, 2H), 4.86 (m, 1H), 5.23 (s, 2H), 5.29-5.38 (m, 1H), 6.85-7.01 (m, 3H), 7.10-7.84 (m, 10H), 7.96 (s, 1H). Mass spec.: 589.16 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-dbb83d8fe1734b3db0e6e9c4968538a1
Source noteuspto-grants-2009_08