부분 구조 검색

834772

COc1ccc(C2(C(=O)NCCc3c(-c4ccccc4)c4cc(OC)ccc4c(=O)n3C)CC2)cc1
Reaction #46140
titled product
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CO)C[C@@H](O)c1ccccn1
Reaction #51921
title compound
수율 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CO)CC(O)c1ccc2ccccc2n1
Reaction #51927
title compound
수율 98.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CN)C[C@@H](O)c1ccccn1
Reaction #51931
amine
수율 78.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CNS(C)(=O)=O)C[C@@H](O)c1ccccn1
Reaction #51932
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccc3ccccc3n2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51963
title compound
수율 59.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(n1)C(C(=O)N(Cc1ccc(N(C)C)cc1)c1ccc(C(C)C)cc1)CCC2
Reaction #62049
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1ccccn1
Reaction #83133
product
수율 72186.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cccc(C3CNCCC3(F)F)n2)n1
Reaction #86254
259
수율 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccc(N3CCN(C)CC3)nc2)cc2c1cnn2C(C)C
Reaction #90711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #91527
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(CN(CC(=O)c2ccccn2)Cc2ccccc2)CC1
Reaction #160067
tert-butyl 4-[[benzyl-[2-oxo-2-(2-pyridyl)ethyl]amino]methyl]-4-hydroxy-piperidine-1-carboxylate
수율 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN(Cc1ccccc1)C=C(c1ccccn1)O2
Reaction #160068
tert-butyl 8-benzyl-10-(2-pyridyl)-11-oxa-3,8-diazaspiro[5.5]undec-9-ene-3-carboxylate
수율 47.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2c1C(=O)N(C(=O)OC(C)(C)C)CC2
Reaction #168007
tert-butyl 2-chloro-4-methyl-5-oxo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CN(S(=O)(=O)c3ccc(Cl)c(Cl)c3)Cc3cccnc3[C@@H]2C1
Reaction #172149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C)[nH]c(=O)c1CNC(=O)c1cc(-c2ccc(N3CCN(C)CC3)nc2)cc2c1cnn2C(C)C
Reaction #172618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CC(c2cc(NC(=O)C(C)(C)c3ccccn3)n(C(C)(C)C)n2)C1
Reaction #173244
DOI: 10.1039/C8SC04228D
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CNS(C)(=O)=O)CC(O)c1ccccn1
Reaction #184785
DOI: 10.1039/C8SC04228D
CN(Cc1sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c2c1CO)CC(O)c1ccc2ccccc2n1
Reaction #185223
DOI: 10.1039/C8SC04228D
O=C(Nc1nc(-c2ccc(-n3ccnn3)cc2)c(Cl)s1)N(CCc1ccccn1)CCC(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #192552
DOI: 10.1039/C8SC04228D
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