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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactantmethyl 1H-indole-4-carboxylateHCID 2733668—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1,5-Dihydro-3-phenyl-[1,2]diazepino[4,5,6-cd]-indol-6-oneHCID 135463034—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
Product1,5-Dihydro-3-methyl-[1,2]diazepino[4,5,6-cd]-indol-6-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977298B2
Source datasetuspto-grants-2005_12
ORD IDord-4a3cbb594f9c4b9ca4447a8f162464ec
Source noteuspto-grants-2005_12