HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307365Generated: October 31, 2026
Diisopropylethylamine → HCID 9929208, compound
https://huagongshe.com/reaction/2307365
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepine | HCID 15547048 | — |
| Reactant | 4-(4-Methyl-1H-imidazol-1-yl)benzoyl chloride | HCID 22605434 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9929208 | HCID 9929208 | 40.6% |
Reaction Steps
The 4-(4-methylimidazol-1-yl)benzoyl chloride (0.99 g) was added to an ice-cooled solution of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine (0.64 g) and diisopropylethylamine (0.60 g) in dichloromethane (25 ml). After stirring at room temperature for 18 hours, the reaction mixture was washed with water and saturated aqueous sodium bicarbonate. The dichloromethane solution was dried over anhydrous sodium sulfate, filtered through a short column of hydrous sodium magnesium silicate, and further eluted with several volumes of dichloromethane. The combined organic phase was concentrated on a hot plate with the gradual addition of hexane until crystallization occurred. After cooling, the title compound (0.52 g) was obtained as a solid, m.p. 140-145° C.; MS, m/z: 369 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831079B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-c1b41074b3814ee7b9187b8dd7899673 |
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| Source note | uspto-grants-2004_12 |
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