부분 구조 검색

758276

CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3cccc(Cl)c3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43866
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3cccc(Cl)c3)ccc2n1CC(=O)O
Reaction #43867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3ccc(Cl)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43868
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3ccc(Cl)cc3)ccc2n1CC(=O)O
Reaction #43869
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cl)cc(C(=O)N(CCc2cc(F)cc(C(F)(F)F)c2)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #48091
N-(4-tert-butyl-benzyl)-3-chloro-N-[2-(3-fluoro-5-trifluoromethyl-phenyl)-ethyl]-5-propyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #49125
hydrochloride salt
수율 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)N1Cc2c(Cl)c(O)cc(I)c2C1=O
Reaction #49538
4-chloro-5-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
수율 108.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)c(O)cc(I)c21
Reaction #49539
4-chloro-5-hydroxy-7-iodoisoindolinone
수율 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(c1ccc(Cl)cc1)N(CCc1ccccc1)Cc1ccccc1OCCN1CCOCC1
Reaction #55246
material
수율 168.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccccc2F)CC1
Reaction #60712
3-Chloro-N-[1-(2-fluorophenyl)-2-(1-methylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2c(C(=O)N(Cc3ccc(OC)cc3)Cc3ccc(OC)cc3)c(=O)[nH]c3ccccc23)cc1
Reaction #72684
N,N-bis(4-methoxybenzyl)-4-(4-methoxybenzylamino)-2-oxo-1,2-dihydroquinoline-3-carboxamide
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(Cc2ccc(OC)cc2)C(=O)c2c(Cl)c3ccccc3[nH]c2=O)cc1
Reaction #72685
4-chloro-N,N-bis(4-methoxybenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxamide
수율 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(CN(CCc2cccc(Cl)c2F)C(=O)c2cccc3cc[nH]c23)cc1
Reaction #174648
DOI: 10.1039/C8SC04228D
O=C1c2cc(Cl)ccc2CN1Cc1ccccc1
Reaction #179577
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(CN(CCc2ccc(F)c(Cl)c2)C(=O)c2c(F)c(Cl)cc3cc[nH]c23)cc1
Reaction #181071
DOI: 10.1039/C8SC04228D
O=C([O-])c1ccc(C2(NC(=O)c3cccc4c3N(Cc3ccc(Cl)c(Cl)c3)CC4)CC2)cc1
Reaction #181418
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(CN(CCc2ccncc2)C(=O)c2cc(Cl)cc3cc[nH]c23)cc1
Reaction #184070
DOI: 10.1039/C8SC04228D
CCOC(=O)COc1cc(Oc2ccc(CN(Cc3ccccc3F)c3cccc(N)c3C)cc2)ccc1Cl
Reaction #186852
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(-c2cc[nH]c(=O)c2)cc1)c1c(F)ccc(F)c1Cl
Reaction #196523
DOI: 10.1039/C8SC04228D
CCOC(=O)COc1cc(Oc2ccc(CN(Cc3ccccc3F)c3cccc([N+](=O)[O-])c3C)cc2)ccc1Cl
Reaction #201368
DOI: 10.1039/C8SC04228D
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