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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(1-Pyrrolidinyl)piperidine | HCID 78703 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10223535 | HCID 10223535 | — |
| Reactant | HCID 18449085 | HCID 18449085 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10187539 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202239B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-22b9044df12a4ecabc876a659477356e |
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| Source note | uspto-grants-2007_04 |
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