部分構造検索

625660

CC(C)(C)OC(=O)NN1CCN(C(=O)CBr)C1=O
Reaction #4214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NN1CCN(C(=O)CI)C1=O
Reaction #4215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](NC(=O)OCc2ccccc2)C(=O)N1P(=O)(O)OCC(=O)N1CCN(N)C1=O
Reaction #4216
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCNC(=O)OCc1ccccc1)NCCN1CCCCC1
Reaction #10558
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(NC(=O)N(C)Cc3ccccc3)cnc(CN)c2cc1OC
Reaction #42941
desired product
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCc1ccc([C@H]2NC(=O)N(CC(=O)O)C2=O)cc1
Reaction #49777
(5-(R)-(4-Aminomethylphenyl)-2,4-dioxoimidazolidin-3-yl)-acetic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(I)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50916
405
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50917
406
収率 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)Nc1ccc(-c2ccccc2SC)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50919
409
収率 85.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)n1cc(-c2ccncc2)c(-c2cccc(NC(=O)Nc3ccc(C(F)(F)F)cc3)c2)n1
Reaction #74099
4-pyridin-4-yl-3-{3-[3-(4-trifluoromethyl-phenyl)-ureido]-phenyl}-pyrazole-1-carboxylic acid ethyl ester
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc2c(c1)CCc1cc(OCCOCCOC(=O)NCCOCCOCCNC(=O)CCCCC3SCC4NC(=O)NC43)ccc1C#C2
Reaction #74292
6b
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CN(C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc2ccno2)co1
Reaction #81008
desired compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc(CN(C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc2ccccc2)C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc2ccno2)co1
Reaction #84003
desired compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=O)NC4CC4)c(F)c3)c2cc1NC(=O)OCc1ccccc1
Reaction #177879
DOI: 10.1039/C8SC04228D
CCCCC(NC(=O)OC(Cn1ccc(-c2ccc(C(F)(F)F)cc2)n1)C(C)(C)C)C(O)CNC(=O)N1CCOCC1
Reaction #179242
DOI: 10.1039/C8SC04228D
C=C1C(=O)N(c2ccc(C#N)c(Cl)c2C)C(=O)N1C
Reaction #179814
DOI: 10.1039/C8SC04228D
CNC(=O)OC1CN(C(=O)N(C)C)CC1Oc1ccc(Cl)cc1
Reaction #182616
DOI: 10.1039/C8SC04228D
Cc1cn(C(=O)NC(CCCNC(=O)OC(C)(C)C)C(=O)O)c(=O)[nH]c1=O
Reaction #184904
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCC1CCCN(C(N)=O)C1
Reaction #187207
DOI: 10.1039/C8SC04228D
CCOC(=O)NNC(=O)Nc1c(F)cc(F)cc1F
Reaction #189591
DOI: 10.1039/C8SC04228D
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