Methyl 3-(4-chloro-5,6,7,8-tetrahydro-[1]benzothieno[2,3-d]pyrimidin-2-yl)propionate → 3-[4-(Cyclopropyl-methyl-amino)-5,6,7,8-tetrahydro-[1]benzothiopheno[2,3-d]pyrimidin-2-yl]-propionic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:20])[CH2:4][CH2:5][C:6]1[N:7]=[C:8](Cl)[C:9]2[C:14]3[CH2:15][CH2:16][CH2:17][CH2:18][C:13]=3[S:12][C:10]=2[N:11]=1.Cl.[CH:22]1([NH:25][CH3:26])[CH2:24][CH2:23]1>CO>[CH3:1][O:2][C:3](=[O:20])[CH2:4][CH2:5][C:6]1[N:7]=[C:8]([N:25]([CH:22]2[CH2:24][CH2:23]2)[CH3:26])[C:9]2[C:14]3[CH2:15][CH2:16][CH2:17][CH2:18][C:13]=3[S:12][C:10]=2[N:11]=1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
The TEA (0.6 g, 0.0064 mol) was added dropwise at 10° C. to a mixture of 3-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiopheno[2,3-d]pyrimidin-2-yl)-propionic acid methyl ester (1 g, 0.0032 mol) and cyclopropyl methyl amine hydrochloride (0.35 g, 0.0032 mol) in methanol (20 ml). The resulting mixture was stirred at R.T for 10 hrs. Methanol was removed and the reaction mixture was diluted with water and extracted with ethyl acetate (3×25 ml). The combined organic layers were dried over Na2SO4, concentrated and subjected to column purification on 60-120 silica using ethyl acetate (50%) in hexane to give 0.5 g (43%) of 3-[4-(cyclopropyl-methyl-amino)-5,6,7,8-tetrahydro-[1]benzothiopheno[2,3-d]pyrimidin-2-yl]-propionic acid methyl ester. 1H NMR (400 MHz, DMSO) δ ppm=0.35 (m, 2H), 0.72 (m, 2H), 1.69 (m, 2H), 1.85 (m, 2H), 2.77 (q, 4H), 2.86 (q, 2H), 2.9 (m, 1H), 2.97 (s, 3H) 3.02 (t, 2H), 3.56 (s, 3H). LC-MS: [M+H]=345.8.