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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270193Generated: November 1, 2026

4-(1-Pyrrolidinyl)piperidine → HCID 10187539, compound

https://huagongshe.com/reaction/1270193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Pyrrolidinyl)piperidineHCID 78703—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 10223535HCID 10223535—
ReactantHCID 18449085HCID 18449085—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 10187539HCID 10187539—

Reaction Steps

A stirred solution of the crude 10-(4-cyclohexyl-benzoyl)-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-3-carbonyl chloride (prepared in the manner of Example 23, from 1 g of the corresponding carboxylic acid of Example 22) in dichloromethane (25 mL) was treated with 4-(1-pyrrolidinyl) piperidine (0.74 g), N,N-diisopropylethyl amine (0.31 g) and 4-(dimethylamino)pyridine (0.05 g). The reaction mixture was stirred at room temperature overnight, washed with water and saturated aqueous sodium bicarbonate and dried over anhydrous sodium sulfate. Filtration of this solution through a short column of Magnesol® gave a pale yellow eluate which was evaporated to dryness to provide the title compound as a pale yellow amorphous material (0.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202239B2
Source datasetuspto-grants-2007_04
ORD IDord-22b9044df12a4ecabc876a659477356e
Source noteuspto-grants-2007_04