반응식
C([N:8]([CH2:23][CH:24]([OH:34])[CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[CH3:33])[C:9]([CH3:22])([CH3:21])[CH2:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([C:18](=[O:20])[NH2:19])=[CH:14][N:13]=1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[C:18]([C:15]1[CH:16]=[CH:17][C:12]([O:11][CH2:10][C:9]([NH:8][CH2:23][CH:24]([OH:34])[CH2:25][O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[CH3:33])([CH3:21])[CH3:22])=[N:13][CH:14]=1)(=[O:20])[NH2:19]참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
A solution of 22 g of crude 1-[N-benzyl-N-[2-(5-carbamoyl-2-pyridyloxy)-1,1-dimethyl-ethyl]-amino]-3-(2-methyl-phenoxy)-2-propanol in 220 ml of methanol is hydrogenated analogously to Example 1, a total of 6 g of palladium-on-charcoal catalyst (5% strength) being added in 2 portions in order that the calculated amount of hydrogen should be taken up. Working up gives an oil from which 1-[2-(5-carbamoyl-2-pyridyloxy)-1,1-dimethyl-ethylamino]-3-(2-methyl-phenoxy)-2-propanol of melting point 122°-128° C. is obtained by crystallisation from ethyl acetate.
출처 및 근거
- ORD 기록
- ord-6fcad40028954a55ba82d62a0d2ecc60
- 출처 데이터셋
- uspto-grants-1977_05
- 특허 번호
- US04027027
연결된 노트
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