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HCID 178488167、化合物 → HCID 178462268、化合物

HRID 2121908
ノート
印刷プレビュー

反応式

HRID 2121908 の反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][N:7]=[C:6]2[CH2:12][C@H:13]([OH:15])[CH3:14]>ClCCl>[OH:15][C@H:13]([CH3:14])[CH2:12][C:6]1[C:5]2[C:9](=[CH:10][CH:11]=[C:3]([OH:2])[CH:4]=2)[NH:8][N: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

3

反応物 1

HCID 178488167HCID 178488167、化合物

生成物 1

HCID 178462268HCID 178462268、化合物収率 70%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of (R)-1-(5-Methoxy-1H-indazol-3-yl)-propan-2-ol (2.31 g, 11.2 mmol) in anhydrous dichloromethane (50 mL) cooled at −78° C. was added a 1 N borontribromide solution in dichloromethane (33.6 mL, 33.6 mmol). After the addition was complete, the mixture was allowed to warm to ambient temperature and stirred for 2 hours. The mixture was cooled (ice bath) and quenched with 20 mL of water. Dichloromethane was evaporated and the residue was mixed with ethyl acetate (100 mL). To this solution potassium carbonate was added in small portions until gas evolution ceased and the pH was about 8. The mixture was extracted with ethyl acetate (3×100 mL) and the combined extracts were dried and evaporated to dryness. Chromatography on silica (gradient, 50% to 90% ethyl acetate in hexane) gave an oil (1.50 g, 70%): LC/MS (+APCI) m/z 193 (M+H).

後処理

  1. additionAfter the addition
  2. temperatureThe mixture was cooled (ice bath)
  3. customquenched with 20 mL of water
  4. customDichloromethane was evaporated
  5. additionthe residue was mixed with ethyl acetate (100 mL)
  6. additionTo this solution potassium carbonate was added in small portions until gas evolution
  7. extractionThe mixture was extracted with ethyl acetate (3×100 mL)
  8. customthe combined extracts were dried
  9. customevaporated to dryness

出典と根拠

ORDレコード
ord-57f84316f70e4b6c8510dd652723e98d
出典データセット
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06696476B2

反応ノート

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