Hydrochloric Acid → (3RS)-1,3-dihydro-3-(2-indolylcarbonylamino)-1-[(2-aminothiazol-4-yl)methyl]-5-phenyl-2H-1,4-benzodiazepine-2-one

HRID 1073714노트

반응식

HRID 1073714 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([NH:12][CH:13]1[N:19]=[C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:17]2[CH:26]=[CH:27][CH:28]=[CH:29][C:16]=2[N:15]([CH2:30][C:31]2[N:32]=[C:33]([NH:36]C(=O)C)[S:34][CH:35]=2)[C:14]1=[O:40])=[O:11].CO.Cl.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.O.O1CCCC1>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([NH:12][CH:13]1[N:19]=[C:18]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[C:17]2[CH:26]=[CH:27][CH:28]=[CH:29][C:16]=2[N:15]([CH2:30][C:31]2[N:32]=[C:33]([NH2:36])[S:34][CH:35]=2)[C:14]1=[O:40])=[O:11]

참가 물질

8

반응 조건

온도
70 °C

실험 절차

A mixture of (3RS)-1,3-dihydro-3-(2-indolylcarbonyl-amino) -1-[(2-acetamidothiazol-4-yl)methyl]-5-phenyl-2H-1,4-benzodiazepine -2-one, methanol (13 ml), tetrahydrofuran (8 ml) and conc. hydrochloric acid (0.8 ml) was stirred for 7.0 hours at 70° C., cooled and adjusted to pH 7.0 with aqueous solution of sodium bicarbonate. To the mixture were added water (100 ml) and ethyl acetate (100 ml) under cooling. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel with an eluent of a mixture of ethyl acetate and chloroform (2:1) to give (3RS)-1,3-dihydro-3-(2-indolylcarbonylamino) -1-[(2-aminothiazol-4-yl)methyl]-5-phenyl -2H-1,4-benzodiazepine-2-one.

후처리

  1. temperaturecooled
  2. temperatureunder cooling
  3. washThe separated organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customThe residue was chromatographed on silica gel with an eluent of a mixture of ethyl acetate and chloroform (2:1)

출처 및 근거

ORD 기록
ord-2151ee3efd634237b1903b360fd19f6a
출처 데이터셋
uspto-grants-1990_11
특허 번호
US04970207

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