Synthesis and medical application of pyrrolo-[2,1-f] [1,2,4] triazine mother nucleus compound
A compound, pyrrole technology, applied in the field of medicinal chemistry, can solve problems such as the incomplete development of BTK inhibitors and narrow clinical indications
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Embodiment 1
[0032] Preparation of pyrrolo[2,1-f][1,2,4]triazine core compound BTK irreversible inhibitor compound (1)
[0033]
[0034] White crystalline powder, M.P.186-188℃. 1 H-NMR (400MHz, DMSO-d 6 )δ:10.17(1H,s),9.02(1H,s),8.67(1H,s),7.15-7.34(2H,m),6.45-6.96(6H,m),6.64(1H,d),6.51 (1H,m),6.17-6.25(2H,m),6.02(1H,d,J=15.6Hz),5.51(1H,d,J=6.8Hz),4.43(2H,t),3.39(2H, t),2.38(2H,t),2.27(3H,s),1.64(2H,m); 13 C-NMR (100MHz, DMSO-d 6 )δ: 166.8, 161.6, 149.5, 142.8, 139.7, 136.8, 131.2, 129.9, 128.6, 126.9, 122.8, 118.2, 113.7, 111.9, 110.3, 108.2, 100.8, 86.6, 58.5, 57.8, 42.4 )calcd.for C 26 h 28 N 8 O[M+H] + ,468.2386; found, 468.2392.
Embodiment 2
[0036] Preparation of Pyrrolo[2,1-f][1,2,4]triazine Core Compound BTK Irreversible Inhibitor Compound (2)
[0037]
[0038] White crystalline powder, M.P.165-167℃. 1 H-NMR (400MHz, DMSO-d 6 )δ:10.33(1H,s),9.25(1H,s),8.79(1H,s),7.19-7.38(2H,m),6.44-6.95(6H,m),6.66(1H,d),6.53 (1H,m),6.16-6.25(2H,m),6.02(1H,d,J=12.5Hz),5.50(1H,d,J=8.7Hz),3.46(4H,t),2.38(4H, t),2.26(3H,s); 13 C-NMR (100MHz, DMSO-d 6 )δ: 166.8, 161.6, 149.5, 142.8, 139.7, 136.8, 131.2, 129.9, 128.6, 126.9, 122.8, 118.2, 113.7, 111.9, 110.3, 108.2, 101.1, 57.4, 52.1, 46.8; C 26 h 28 N 8 O[M+H] +,468.2386; found, 468.2392.
Embodiment 3
[0040] Preparation of pyrrolo[2,1-f][1,2,4]triazine core compound BTK irreversible inhibitor compound (3)
[0041]
[0042] White crystalline powder, M.P.170-172℃. 1 H-NMR (400MHz, DMSO-d 6 )δ:10.29(1H,s),9.18(1H,s),8.82(1H,s),7.18-7.37(2H,m),6.44-6.95(6H,m),6.65(1H,d),6.53 (1H,m),6.16-6.25(2H,m),6.04(1H,d,J=14.4Hz),5.53(1H,d,J=9.8Hz),3.47(4H,t),2.80(4H, t),1.93(1H,s); 13 C-NMR (100MHz, DMSO-d 6 )δ: 166.8, 161.6, 149.5, 142.8, 139.7, 136.8, 131.2, 129.9, 128.6, 126.9, 122.8, 118.2, 113.7, 111.9, 110.3, 108.2, 101.1, 53.8, 45.9; HRMS (ESI) calcd. 25 h 26 N 8 O[M+H] + ,454.2230; found, 454.2235.
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