ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

HCID 89962871、化合物 → 5-[(1R*,2S*)-2-(Benzyloxy)cyclopentyl]-1H-pyrazole

HRID 337971
ノート
印刷プレビュー

反応式

HRID 337971 の反応式
[CH2:1]([O:8][C@H:9]1[CH2:13][CH2:12][CH2:11][C@@H:10]1[C:14]1[N:18](C2CCCCO2)[N:17]=[CH:16][CH:15]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>ClCCl.FC(F)(F)C(O)=O>[CH2:1]([O:8][C@H:9]1[CH2:13][CH2:12][CH2:11][C@@H:10]1[C:14]1[NH:18][N:17]=[CH:16][CH:15]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 89962871HCID 89962871、化合物

生成物 1

HCID 899629205-[(1R*,2S*)-2-(Benzyloxy)cyclopentyl]-1H-pyrazole収率 98.5%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 6422Trifluoroacetic acid溶媒

実験手順

To a solution of the 5-[(1R*,2S*)-2-(benzyloxy)cyclopentyl]-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole (1.15 g, 3.52 mmol) prepared in Example 148a in dichloromethane (10 mL), trifluoroacetic acid (5.0 mL) was added at room temperature, and the reaction solution was stirred for 12 hours. The reaction solution was concentrated, and a saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added to the residue, followed by extraction with ethyl acetate (50 mL). The thus obtained organic layer was washed with saturated saline (50 mL) and dried over anhydrous sodium sulfate. After vacuum concentration, the residue was purified with silica gel chromatography (hexane/ethyl acetate=1:1) to yield the title compound (840 mg, 98%) as a pale yellow oil.

後処理

  1. concentrationThe reaction solution was concentrated
  2. additiona saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added to the residue
  3. extractionfollowed by extraction with ethyl acetate (50 mL)
  4. washThe thus obtained organic layer was washed with saturated saline (50 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationAfter vacuum concentration
  7. customthe residue was purified with silica gel chromatography (hexane/ethyl acetate=1:1)

出典と根拠

ORDレコード
ord-9fdc968379b64065babbd064df17661b
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889741B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート