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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489571생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/489571

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물Perfluoropropionyl chlorideHCID 67911—
반응물methyl 1H-indole-4-carboxylateHCID 2733668—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물1,5-Dihydro-3-phenyl-[1,2]diazepino[4,5,6-cd]-indol-6-oneHCID 135463034—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매1,1-DichloroethaneHCID 6365—
생성물1,5-Dihydro-3-pentafluoroethyl-[1,2]diazepino[4,5,6-cd]-indol-6-oneHCID 135584184—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06977298B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-f3997a6967ca48e8839f7de9ac6390c3
출처 메모uspto-grants-2005_12