HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635848Generated: October 31, 2026
Diisopropylethylamine → HCID 9907301, compound
https://huagongshe.com/reaction/1635848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepine | HCID 15547048 | — |
| Reactant | HCID 22605448 | HCID 22605448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9907301 | HCID 9907301 | — |
Reaction Steps
The 4-(3-methylpyrazol-1-yl)benzoyl chloride was added to an ice-cooled solution of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine (0.55 g) and diisopropylethylamine (0.44 g) in dichloromethane (25 ml). After stirring at room temperature for 18 hours, the reaction mixture was washed with water and a saturated aqueous sodium bicarbonate solution. The dichloromethane solution was dried over anhydrous sodium sulfate and 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 (0.90 g) was obtained as an amorphous solid, MS, m/z: 369 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511974B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-fa9d97e54aef4ccdaf727637351fe0f3 |
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| Source note | uspto-grants-2003_01 |
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