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8alpha-(3,3-Diethylureido)-6-methylergoline-2-carboxylic acid benzyl ester → 8alpha-(3,3-Diethylureido)-6-methylergoline-2-carboxylic acid

HRID 231702
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인쇄 미리보기

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HRID 231702 반응식
C([O:8][C:9]([C:11]1[NH:25][C:24]2[C:26]3[C:12]=1[CH2:13][C@@H:14]1[C@@H:19]([C:20]=3[CH:21]=[CH:22][CH:23]=2)[CH2:18][C@H:17]([NH:27][C:28]([N:30]([CH2:33][CH3:34])[CH2:31][CH3:32])=[O:29])[CH2:16][N:15]1[CH3:35])=[O:10])C1C=CC=CC=1>CO.[Pd]>[CH2:33]([N:30]([CH2:31][CH3:32])[C:28](=[O:29])[NH:27][C@H:17]1[CH2:18][C@H:19]2[C@@H:14]([CH2:13][C:12]3[C:26]4[C:24](=[CH:23][CH:22]=[CH:21][C:20]2=4)[NH:25][C:11]=3[C:9]([OH:10])=[O:8])[N:15]([CH3:35])[CH2:16]1)[CH3:34]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 135590328alpha-(3,3-Diethylureido)-6-methylergoline-2-carboxylic acid benzyl ester

생성물 1

HCID 135590348alpha-(3,3-Diethylureido)-6-methylergoline-2-carboxylic acid수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

104 mg (0.22 mmol) of 8α-(3,3-diethylureido)-6-methylergoline-2-carboxylic acid benzyl ester is dissolved in 20 ml of methanol and, after adding 50 mg of palladium black, hydrogenated for 30 minutes under normal pressure at room temperature. After the catalyst has been filtered off and the mixture concentrated, 8α-(3,3-diethylureido)-6-methylergoline-2-carboxylic acid is obtained in a 100% yield, mp: decomposition starting with 230° C.

후처리

  1. filtrationAfter the catalyst has been filtered off
  2. concentrationthe mixture concentrated

출처 및 근거

ORD 기록
ord-8673d8affaa5406d84ad1d7b1364609b
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04847262

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