부분 구조 검색

Cl.NCCF

Cl.O=C(NCCCSc1ccncc1)C(F)(F)F
Reaction #6197
desired compound
수율 68.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC1CCN(CC2(F)Cn3c(=O)ccc4ncc(F)c2c43)CC1
Reaction #43443
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N
Reaction #43445
isopropylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44427
trans-N-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
수율 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)C(F)(F)F)[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12
Reaction #44435
trans-N-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoro-N-methylacetamide
수율 90.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44436
trans-N-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetimidamide
수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3c(ccc(Cl)c3Cl)Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44440
trans-N-(6,7-dichloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
수율 17.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(Br)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44441
trans-N-(8-bromo-7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
수율 130.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3ccccc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44442
trans-N-(2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
수율 98.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c([N+](=O)[O-])cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44443
trans-N-(7-chloro-8-nitro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
수율 93.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)Oc1ccc(Cl)cc1N1CCC[C@@H](NC(=O)C(F)(F)F)[C@@H]21
Reaction #44459
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3cccc(F)c3[C@H]12)C(F)(F)F
Reaction #44460
title compound
수율 6.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(NC(N)=NCC(F)(F)F)nc1CCCCN.Cl.Cl
Reaction #63084
2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-aminobutyl)-5-methylthiazole dihydrochloride
수율 128.6%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2nc(C(=O)NCCF)c(C(=O)O)s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72232
title compound
수율 41.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CC(O)(C(F)(F)F)N=C2c2ccc(Cl)cc2)cc1
Reaction #80573
2-(4-chlorophenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazole
수율 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2cc(C(F)(F)F)nc2-c2ccc(Cl)cc2)cc1
Reaction #80574
2-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazole
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2=NC(O)(C(F)(F)F)CN2c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80607
2-(3-chloro-4-methoxyphenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-4,5-dihydro-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80608
2-(3-chloro-4-methoxyphenyl)-1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccnc(Cl)n2)cnc1N1CC[C@H](F)C1
Reaction #84140
title compound
수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84141
solid
수율 38.0%DOI: 10.6084/m9.figshare.5104873.v1
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