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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 86642727, 화합물 → HCID 136388709, 화합물

HRID 1678713
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HRID 1678713 반응식
C([O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[N:14][N:15]2[CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][O:19]2)=[CH:11][CH:10]=1)C1C=CC=CC=1.[CH3:24][N:25]([CH3:30])[C:26](=[O:29])[CH2:27][CH3:28]>C1COCC1>[OH:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[N:14][N:15]2[CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][O:19]2)=[CH:11][CH:10]=1.[CH3:24][N:25]([CH3:30])[C:26](=[O:29])[CH2:27][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86642727HCID 86642727, 화합물

생성물 1

HCID 136388709HCID 136388709, 화합물수율 82.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

5% palladium on carbon-STD-type-50% wet with water (224 mg; manufactured by N.E. Chemcat Corp.), and a THF solution of 3-(6-(benzyloxy)-1-(tetrahydro-2H-pyran-2-yl)-indazole-N,N-dimethylpropanamide that can be produced by the method described in Reference Example 51 or the like [6.3 mL; prepared by dissolving 3-(6-(benzyloxy)-1-(tetrahydro-2H-pyran-2-yl)-indazole-N,N-dimethylpropanamide (596 mg) in dehydrated THF (7.3 mL)) were mixed, and the reaction system was purged with hydrogen. Under a hydrogen atmosphere, the reaction solution was stirred overnight at room temperature. The reaction solution was purged with nitrogen, and then was filtered. The solvent was evaporated under reduced pressure from the filtrate, and thus the title compound (383 mg) was obtained.

후처리

  1. customprepared
  2. additionwere mixed
  3. customthe reaction system was purged with hydrogen
  4. customThe reaction solution was purged with nitrogen
  5. filtrationwas filtered
  6. customThe solvent was evaporated under reduced pressure from the filtrate

출처 및 근거

ORD 기록
ord-96969986e8bf49a782999f66c40ad73d
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008506B2

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