HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489530Generated: October 27, 2026
Acetyl chloride → 1,5-Dihydro-3-methyl-[1,2]diazepino[4,5,6-cd]-indol-6-one
https://huagongshe.com/reaction/489530
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | methyl 1H-indole-4-carboxylate | HCID 2733668 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1,5-Dihydro-3-phenyl-[1,2]diazepino[4,5,6-cd]-indol-6-one | HCID 135463034 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1,5-Dihydro-3-methyl-[1,2]diazepino[4,5,6-cd]-indol-6-one | HCID 135584183 | — |
Reaction Steps
In a manner similar to that described for compound 28, a solution of methyl indole-4-carboxylate (427 mg, 2.44 mmol) in dichloroethane (7 mL) was treated with acetyl chloride (0.5 mL) and aluminum chloride (130 mg). The intermediate ketone (198 mg, 0.92 mmol) in MeOH (5 mL) and conc. HCl (0.05 mL) was treated, as described, with hydrazine hydrate (0.1 mL). The product precipitated, was collected by filtration and rinsed with ice-cold MeOH to give 1,5-dihydro-3-methyl-[1,2]diazepino[4,5,6-cd]-indol-6-one, 168 mg (92%) as a bright yellow solid: m.p. 335-336° C.; 1H NMR (300 MHz, d6-DMSO) δ 2.17 (s, 3H), 7.19 (t, J=7.8 Hz, 1H), 7.54 (m, 2H), 7.67 (d, J=2.8Hz, 1H), 10.12 (s, 1H), 11.90 (br s, 1H). HRMS (FAB, MH+) Calcd for C11H10N3O: 200.0824. Found: 200.0827. Anal. (C11H9N3O) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06977298B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-4a3cbb594f9c4b9ca4447a8f162464ec |
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| Source note | uspto-grants-2005_12 |
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