部分構造検索

1262728

Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)cc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562074
title compound
収率 31.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2c3c(c4ccc(-n5ccc(-c6ccc(C(F)(F)F)nn6)cc5=O)cc42)CCN(C(=O)OC(C)(C)C)CC3)cc1
Reaction #562076
title compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)cc31)CN(C(=O)OC(C)(C)C)CCC2
Reaction #562094
title compound
収率 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)cc31)CNCCC2
Reaction #562095
title compound
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2[nH]c3cc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)ccc3c2C1
Reaction #562110
tert-butyl 8-(2-oxo-4-(6-(trifluoromethyl)pyridazin-3-yl)pyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate
収率 19.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1cc(-c2ccc(C(F)(F)F)nn2)ccn1-c1ccc2c3c([nH]c2c1)CCCNC3
Reaction #562111
title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CCN(C(=O)OC(C)(C)C)CC2
Reaction #562155
title compound
収率 24.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CCNCC2
Reaction #562156
title compound
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CN(C(=O)OC(C)(C)C)CC2
Reaction #969207
title compound
収率 44.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CNCC2
Reaction #969208
title compound
収率 68.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)nc31)CNCC2
Reaction #969209
title compound
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)cc31)CN(C(=O)OC(C)(C)C)CC2
Reaction #1017854
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2[nH]c3cc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)ccc3c2C1
Reaction #1017887
title compound
収率 30.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c3ccc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)cc31)CN(C(=O)OC(C)(C)C)CC2
Reaction #1107769
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2[nH]c3cc(-n4ccc(-c5ccc(C(F)(F)F)nn5)cc4=O)ccc3c2C1
Reaction #1107803
title compound
収率 30.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2ccc(C(F)(F)F)nn2)cc[nH]1
Reaction #1608649
title compound
収率 110.3%DOI: 10.6084/m9.figshare.5104873.v1