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17beta-Carbamoyl-5alpha-androst-2-en-11-one → 17beta-Cyano-5alpha-androst-2-en-11-one

HRID 267637
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HRID 267637 반응식
[C:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]2[C@H:10]3[C@H:20]([C:21](=[O:23])[CH2:22][C@:5]12[CH3:6])[C@:18]1([CH3:19])[C@H:13]([CH2:14][CH:15]=[CH:16][CH2:17]1)[CH2:12][CH2:11]3)(=O)[NH2:2]>C(Cl)(Cl)Cl>[C:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]2[C@H:10]3[C@H:20]([C:21](=[O:23])[CH2:22][C@:5]12[CH3:6])[C@:18]1([CH3:19])[C@H:13]([CH2:14][CH:15]=[CH:16][CH2:17]1)[CH2:12][CH2:11]3)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 8673314617beta-Carbamoyl-5alpha-androst-2-en-11-one

생성물 1

HCID 8673314517beta-Cyano-5alpha-androst-2-en-11-one수율 56.1%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

17β-Carbamoyl-5α-androst-2-en-11-one (4.0g., 13 mmole) and polyphosphate ester (20g.) were refluxed in chloroform (200 ml.) for 20 hr. The chloroform was removed by evaporation and the residue stirred with aqueous 10% sodium carbonate (150 ml.) for an hour. The mixture was extracted with ether and the extract washed (H2O), dried filtered and evaporated to give a solid which, after recrystallisation from chloroform/cyclohexane, gave the title compound (2.17g); m.p. 189°-191°; [α]D + 152°, (c 0.9).

후처리

  • customThe chloroform was removed by evaporation
  • extractionThe mixture was extracted with ether
  • washthe extract washed (H2O)
  • customdried
  • filtrationfiltered
  • customevaporated
  • customto give a solid which
  • customafter recrystallisation from chloroform/cyclohexane
  • 출처 및 근거

    ORD 기록
    ord-038dff8679e547fc81cedbb1e9756d27
    출처 데이터셋
    uspto-grants-1976_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03943124

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