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Hydrazine hydrate (1:1) → (2S)-2-(4-Fluorophenyl)propan-1-amine

HRID 2276739
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HRID 2276739 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([CH3:21])[CH2:9][N:10]2C(=O)C3C(=CC=CC=3)C2=O)=[CH:4][CH:3]=1.O.NN>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C@H:8]([CH3:21])[CH2:9][NH2:10])=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 67453498(S)-2-(2-(4-Fluorophenyl)propyl)isoindoline-1,3-dione

생성물 1

HCID 28267524(2S)-2-(4-Fluorophenyl)propan-1-amine수율 100.2%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
80 °C

실험 절차

To a room-temperature solution of (S)-2-(2-(4-fluorophenyl)propyl)isoindoline-1,3-dione (900 mg, 3.2 mmol, 1.0 equiv) in toluene (14 mL) was added hydrazine hydrate (1.4 mL, 45 mmol, 14 equiv) by syringe. The resulting mixture was heated to 80° C. for 30 minutes and then cooled to room temperature. The resulting solution was decanted from the solid in the reaction mixture, and the solid was washed with additional toluene. The combined organic layers were combined and concentrated in vacuo to provide the title compound (491 mg, 99%), which was used without further purification.

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후처리

  1. temperaturecooled to room temperature
  2. customThe resulting solution was decanted from the solid in the reaction mixture
  3. washthe solid was washed with additional toluene
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-623998cec767480fbf85f2f631c5d2e7
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133123B2

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