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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33348Generated: October 25, 2026

Hydrazine hydrate (1:1) → 1,5-Dihydro-3-pentafluoroethyl-[1,2]diazepino[4,5,6-cd]-indol-6-one

https://huagongshe.com/reaction/33348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantPerfluoropropionyl chlorideHCID 67911—
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-pentafluoroethyl-[1,2]diazepino[4,5,6-cd]-indol-6-oneHCID 135584184—

Reaction Steps

In a manner similar to that described for Compound 28, a solution of methyl indole-4-carboxylate (351 mg, 2.01 mmol) in dichloroethane (7 mL) was treated with pentafluoropropionyl chloride (2.51 mmol) and aluminum chloride (575 mg). The intermediate ketone (50 mg, 0.16 mmol) in MeOH (2 mL) and conc. HCl (0.02 mL) was treated, as described, with hydrazine hydrate (0.1 mL). The reaction was quenched at 0° C. with 1 M NaOAc and the aqueous layer was adjusted to pH=8 with 1 M NaOH. The product was isolated by extraction with CH2Cl2, and recrystallized (CH2Cl2/MeOH/hexanes) to give 1,5-dihydro-3-pentafluoroethyl-[1,2]diazepino[4,5,6-cd]-indol-6-one, 15 mg (28%) as a yellow solid: 1H NMR (300 MHz, d6-DMSO) δ 7.16 (app br t, 1H), 7.54 (m, 2H), 7.65 (m, 1H), 10.87 (s, 1H), 12.15 (s, 1H). HRMS (FAB, Mna+) Calcd for C11H10N3Ona: 352.0674. Found: 352.0668.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429578B2
Source datasetuspto-grants-2008_09
ORD IDord-1ba24dfa03ec499e87362848e609bad5
Source noteuspto-grants-2008_09