HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244260Generated: November 3, 2026
N,N-Dimethylaniline → HCID 68686100, compound
https://huagongshe.com/reaction/2244260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | 10-[(4-Bromophenyl)sulfonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine | HCID 68687871 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68686100 | HCID 68686100 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678787B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-e686264d6c1542fb9c8a4be9bca9c280 |
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| Source note | uspto-grants-2010_03 |
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