Thienothio compound and application thereof
A compound, thiophene technology, applied in the field of medicine, can solve problems such as reduced bioavailability and prolongation of cardiac QT interval
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Embodiment 1
[0025] Example 1: 1-(7-bromo-1,4-dihydrothieno[3',2':5,6]thiapyro[4,3-c]pyrazole-3-carbonyl)-4- Preparation of (4-methylphenyl)piperazine (compound number 01)
[0026] Step A: Preparation of 5,6-dihydro-4H-thieno[2,3-b]thiopyran-4-one
[0027] Add 4.64g (0.04mol) 2-mercaptothiophene and 80mL tetrahydrofuran into a 100mL round bottom flask, add 11mL triethylamine dropwise with stirring, then add 3.3mL acrylic acid, and heat to reflux for 12h. After the reaction was completed, tetrahydrofuran was distilled off. After cooling, 40 mL of ethyl acetate and 20 mL of water were added, the pH was adjusted to 2 with 18% hydrochloric acid, and the organic layer was collected. The aqueous layer was extracted with ethyl acetate, and the organic layers were combined and dried over anhydrous magnesium sulfate. After suction filtration, the filtrate was evaporated to remove the solvent, and a brown solid was precipitated after cooling. Petroleum ether was recrystallized to obtain a white ...
Embodiment 2
[0046] Example 2: 1-(7-bromo-1,4-dihydrothieno[3',2':5,6]thiapyrano[4,3-c]pyrazole-3-carbonyl)-4- Preparation of (diphenylmethyl)piperazine (compound number 02)
[0047] According to the method of Example 1, 1-(7-bromo-1,4-dihydrothieno[3',2':5,6]thiopyrano[4,3-c]pyrazole-3-carbonyl was obtained )-4-(diphenylmethyl)piperazine 0.77g, yield 35%. m.p.: 175-176℃; IR(KBr,cm -1 ):3420,2921,2851,1607,1451,1384,1262,1154,1027,997,877,831,705; 1 H-NMR (600MHz, CDCl 3 ):δ2.44(4H,m),3.79(4H,m),4.16(2H,s),4.25(1H,s),7.19(2H,d,J=8.4Hz),7.28(4H,dd, J=7.2Hz,8.4Hz),7.41(4H,d,J=7.2Hz); ESI-MS(m / z):551.2[M+H] + .
Embodiment 3
[0048] Example 3: N,N-diethyl-7-bromo-1,4-dihydrothieno[3',2':5,6]thiapyrano[4,3-c]pyrazole-3- Preparation of amides (compound number 03)
[0049] According to the method of Example 1, N,N-diethyl-7-bromo-1,4-dihydrothieno[3',2':5,6]thiopyrano[4,3-c]pyridine was prepared Azole-3-amide (Compound No. 03) 0.75 g, yield 50%. m.p.:147-148℃;IR(KBr,cm -1 ):3212,2958,2917,2849,1735,1583,1535,1508,1485,1461,1375,1215,1159,967,849; 1 H-NMR (600MHz, CDCl 3 ):δ1.25(6H,m),3.54(4H,m),4.12(2H,s),7.72(1H,s); ESI-MS(m / z):372.0,374.0[M+H] + .
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