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3-(3-nitro-1H-pyrazol-1-yl)propan-1-ol → 3-(3-amino-1H-pyrazol-1-yl)propan-1-ol

HRID 546018
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HRID 546018 반응식
[N+:1]([C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][CH2:11][OH:12])[N:5]=1)([O-])=O>O1CCCC1.NN.[Ni]>[NH2:1][C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][CH2:11][OH:12])[N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 196218383-(3-nitro-1H-pyrazol-1-yl)propan-1-ol

생성물 1

HCID 509897073-(3-amino-1H-pyrazol-1-yl)propan-1-ol

시약·촉매·용매 3

HCID 935Nickel촉매HCID 8028Tetrahydrofuran용매2회HCID 9321Hydrazine용매

실험 절차

To a solution containing 3-(3-nitro-pyrazol-1-yl)-propan-1-ol (72 mg, 0.42 mmol) in tetrahydrofuran (2 mL), anhydrous hydrazine (100 μL) was added to the clear solution. Raney nickel (˜100 mg washed 3 times with 5 mL of anhydrous tetrahydrofuran) was then added in tetrahydrofuran (300 μL). Gas evolved from the mixture and the reaction was allowed to proceed for 5 min, after which time the raney nickel was removed by filtration through a celite plug. The solvent was removed in vacuo to afford 3-(3-amino-pyrazol-1-yl)-propan-1-ol as a yellow oil, which was then immediately used in the next step with no further purification.

후처리

  1. additionwas added to the clear solution
  2. customafter which time the raney nickel was removed by filtration through a celite plug
  3. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-1afc62dd100c452589fec169a08eb4d5
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935699B2

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