3-[1-(7-Benzyloxy-6-methoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-1,6-dimethyl-2,4-dioxoquinazoline → 1,2,3,4-Tetrahydro-3-[1-(7-hydroxy-6-methoxy-4-quinazolinyl)-4-piperidinyl]-1,6-dimethyl-2,4-dioxo-quinazoline
반응식
C([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([N:19]3[CH2:24][CH2:23][CH:22]([N:25]4[C:34](=[O:35])[C:33]5[C:28](=[CH:29][CH:30]=[C:31]([CH3:36])[CH:32]=5)[N:27]([CH3:37])[C:26]4=[O:38])[CH2:21][CH2:20]3)=[N:14][CH:15]=[N:16]2)=[CH:11][C:10]=1[O:39][CH3:40])C1C=CC=CC=1>C(O)C.[Pd]>[OH:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([N:19]3[CH2:24][CH2:23][CH:22]([N:25]4[C:34](=[O:35])[C:33]5[C:28](=[CH:29][CH:30]=[C:31]([CH3:36])[CH:32]=5)[N:27]([CH3:37])[C:26]4=[O:38])[CH2:21][CH2:20]3)=[N:14][CH:15]=[N:16]2)=[CH:11][C:10]=1[O:39][CH3:40]참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
In 10 ml of ethanol was dissolved 150 mg (0.28 mmol) of Compound 87 obtained in Example 66, and 30 mg of 10% palladium on carbon was added thereto, followed by vigorous stirring at room temperature for 6 hours under a hydrogen atmosphere at atmospheric pressure. The reaction mixture was filtered using a filter aid, and the filtrate was concentrated under reduced pressure. To the residue were added ethanol and ethyl acetate. The precipitated crystals were collected by filtration, washed, and dried to give 105.2 mg (yield: 84%) of Compound 89 as white crystals.