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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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trans-3-Cyclopropylmethoxy-4-azidotetrahydrofuran → trans-3-Cyclopropylmethoxy-4-aminotetrahydrofuran

HRID 398391
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HRID 398391 반응식
[CH:1]1([CH2:4][O:5][C@H:6]2[C@H:10]([N:11]=[N+]=[N-])[CH2:9][O:8][CH2:7]2)[CH2:3][CH2:2]1>CCOC(C)=O.[Pd]>[CH:1]1([CH2:4][O:5][C@H:6]2[C@H:10]([NH2:11])[CH2:9][O:8][CH2:7]2)[CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 131724050trans-3-Cyclopropylmethoxy-4-azidotetrahydrofuran

생성물 1

HCID 70024767trans-3-Cyclopropylmethoxy-4-aminotetrahydrofuran

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

A solution of trans-3-cyclopropylmethoxy-4-azidotetrahydrofuran from step 3 above (1.2 g, mmol, 6.55 mmol) and 10% Pd on carbon (150 mg) in EtOAc (35 mL) was stirred under an atmosphere of hydrogen at ambient pressure and ambient temperature for 6 h. The catalyst was removed by filtration and the filtrate solvents were removed in vacuo to give the title compound as an oil (1.1 g, TLC Rf=0.3, 95:5:0.25 CH2Cl2:MeOH:NH4OH).

후처리

  1. customThe catalyst was removed by filtration
  2. customthe filtrate solvents were removed in vacuo

출처 및 근거

ORD 기록
ord-85099aea01ea450ea620184891a84ca8
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06610692B1

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