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HCID 86642727、化合物 → HCID 136388709、化合物

HRID 1678713
ノート
印刷プレビュー

反応式

HRID 1678713 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 86642727HCID 86642727、化合物

生成物 1

HCID 136388709HCID 136388709、化合物収率 82.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-96969986e8bf49a782999f66c40ad73d
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08008506B2

反応ノート

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