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Hydrazine hydrate (1:1) → HCID 21975635, 화합물

HRID 640969
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HRID 640969 반응식
[F:1][CH:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[CH:13][CH:12]=2)[CH2:3]1.O.NN>C(O)C.[Ni]>[F:1][CH:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:12]=[CH:13][C:14]([NH2:17])=[CH:15][CH:16]=2)[CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 68696157HCID 68696157, 화합물

생성물 1

HCID 21975635HCID 21975635, 화합물

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

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온도
50 °C

실험 절차

A solution of crude 3-Fluoro-1-[3-(4-nitro-phenoxy)-propyl]-pyrrolidine (6.316 g, ˜24 mmol) was dissolved in absolute ethanol (180 mL) and to this solution was added hydrazine monohydrate (˜7.9 mL) followed by the addition of a small portion of Raney nickel (˜1 mL). The reaction mixture was heated to 50° C. with stirring for ˜2 h at which point all gas evolution had ceased. The reaction mixture was filtered through celite to remove the Raney nickel. The filtrate was concentrated in vacuo to give 4-[3-(3-Fluoro-pyrrolidin-1-yl)-propoxy]-phenylamine as a brown oil which was subjected to flash silica gel chromatography (CHCl3 to CHCl3:MeOH, 1:40 gradient eluant). Pure 4-[3-(3-Fluoro-pyrrolidin-1-yl)-propoxy]-phenylamine was isolated as a reddish oil (4.033 g, 79%).

후처리

  1. filtrationThe reaction mixture was filtered through celite
  2. customto remove the Raney nickel
  3. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-93f44423b2f44b74815b493e081a9e0b
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07692005B2

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