HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356144Generated: October 25, 2026
Sodium hydride → 9-(4-Nitrobenzyl)-2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one
https://huagongshe.com/reaction/356144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | 2,3,9,10a-Tetrahydro-1H-benzo[b]cyclopenta[f][1,4]diazepin-10-one | HCID 12394935 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-(4-Nitrobenzyl)-2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one | HCID 70112964 | 71% |
Reaction Steps
A suspension of 2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (25.00 g, 0.125 mol.) in N,N-dimethylformamide (150 mL) was cooled to 0° C., to which was added sodium hydride (60% liquid paraffin dispersion, 5.00 g, 0.125 mol.). This mixture was stirred for 10 minutes at the same temperature and for 5 minutes at 20° C. This solution was cooled to 0° C., to which was added 4-nitrobenzyl bromide (28.32 g, 0.131 mol.), and the mixture was stirred for 10 minutes at 20° C. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride (500 mL). Resulting precipitate was subjected to filtration, and washed with water, followed by recrystallization from dichloromethane-ethanol to give 29.76 g (yield 71%) of the titled compound. The sample for analylical experiment was prepared by recrystallization of the compound from chloroform-ethanol, m.p. 185°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834463 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-986ae27d19904754ad8ec8c82ad9b3f0 |
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| Source note | uspto-grants-1998_11 |
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