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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244260Generated: November 3, 2026

N,N-Dimethylaniline → HCID 68686100, compound

https://huagongshe.com/reaction/2244260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant10-[(4-Bromophenyl)sulfonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 68687871—
SolventDichloromethaneHCID 6344—
ProductHCID 68686100HCID 6868610063%

Reaction Steps

To a solution of 10-[(4-bromophenyl)sulfonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine of Step A (2.32 g, 5.753 mmol) and N,N-dimethylaniline (1.17 mL, 9.204 mmol) in dry dichloromethane (20 mL) at 0° C. under nitrogen was added dropwise trichloroacetyl chloride (0.96 mL, 8.629 mmol). The ice bath was removed and the reaction mixture stirred at room temperature for 21 hours. The reaction mixture was then washed with 2 M hydrochloric acid (2×100 mL) and water (100 mL), dried over anhydrous magnesium sulfate, and concentrated in vacuo to give an olive foam. Purification by flash chromatography using a solvent gradient of 5-15% ethyl acetate in hexane afforded a cream solid that was recrystallized from diethyl ether/hexane to afford the title compound (1.986 g, 63%) as an off-white crystalline solid, m.p. 182-183 ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678787B2
Source datasetuspto-grants-2010_03
ORD IDord-e686264d6c1542fb9c8a4be9bca9c280
Source noteuspto-grants-2010_03