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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178488167, 화합물 → HCID 178462268, 화합물

HRID 2121908
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HRID 2121908 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178488167HCID 178488167, 화합물

생성물 1

HCID 178462268HCID 178462268, 화합물수율 70%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-57f84316f70e4b6c8510dd652723e98d
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06696476B2

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