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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(-) (2aR,4S)-6-(2-oxazolyl)-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole → (-) (4R)-6-(2-oxazolyl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole

HRID 1598284
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HRID 1598284 반응식
[O:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1[CH:14]=[CH:13][C:12]2[NH:11][CH2:10][C@@H:9]3[CH2:15][C@H:16]([N:18]([CH2:22][CH2:23][CH3:24])[CH2:19][CH2:20][CH3:21])[CH2:17][C:7]=1[C:8]=23>C(Cl)Cl.O=[Mn]=O>[O:1]1[CH:5]=[CH:4][N:3]=[C:2]1[C:6]1[CH:14]=[CH:13][C:12]2[NH:11][CH:10]=[C:9]3[CH2:15][C@H:16]([N:18]([CH2:22][CH2:23][CH3:24])[CH2:19][CH2:20][CH3:21])[CH2:17][C:7]=1[C:8]=23
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참가 물질

4

반응물 1

HCID 18654736(-) (2aR,4S)-6-(2-oxazolyl)-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole

생성물 1

HCID 10663705(-) (4R)-6-(2-oxazolyl)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole수율 37.1%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

A solution of 0.65 g (2.0 mmol) of (-)(2aR,4S)-6-(2-oxazolyl)-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole in 30 ml of CH2Cl2 was sonicated (50-55 KHz) in the presence of 2.5 g of MnO2 for 5 hours. The oxidant was removed by filtration through celite. The crude product obtained after filtering and removing the solvent was chromatographed over 15 g of silica gel using 1:9 EtOAc/toluene, then crystallized from isooctane to provide 0.24 g of title compound.

후처리

  1. customThe oxidant was removed by filtration through celite
  2. customThe crude product obtained
  3. filtrationafter filtering
  4. customremoving the solvent
  5. customwas chromatographed over 15 g of silica gel using 1:9 EtOAc/toluene
  6. customcrystallized from isooctane

출처 및 근거

ORD 기록
ord-fe11132faa984df493c6c8b0bd49c726
출처 데이터셋
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05736562

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