部分構造検索

16955

CCC(NC(=O)C1CCC1)c1nnc(C2CC2)[nH]c1=O
Reaction #7637
N-[1-(3-Cyclopropyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CCC1)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7639
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1CCC1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41325
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(OC(=O)C2CCC2)c(F)c1-c1ccccc1
Reaction #45776
compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1nnc[nH]c1=O)C1CCC1
Reaction #46256
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(C(=O)Cl)C1
Reaction #55572
title compound
収率 60.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc2ccc(-c3cccc(NC(=O)C4CCC4)c3)nn12
Reaction #63910
crystals
収率 25.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)C2CCC2)sc1C(=O)NCc1ccccc1
Reaction #73608
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1cccc2ccccc12)C1CCC1
Reaction #80567
N-[2-(1-naphthyl)ethyl]cyclobutanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C1CCC1
Reaction #87844
desired product
収率 16.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cnc(C(F)F)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C1CCC1
Reaction #87850
desired product
収率 22.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnco2)cc1)N(C1CC1)C1CCN(c2noc(C3CCC3)n2)CC1
Reaction #156030
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNc1ccccc1)C1CCC1
Reaction #161700
Cyclobutanecarboxylic acid N′-phenylhydrazide
DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CC(N2CCCCC2Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162058
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)C1CCC1)C(Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #182948
DOI: 10.1039/C8SC04228D
Cl
Reaction #184740
DOI: 10.1039/C8SC04228D
Cl
Reaction #187513
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(-c2ccc(C(F)(F)F)cc2CN(CC)C(=O)C2CCC2)c1
Reaction #188166
DOI: 10.1039/C8SC04228D
CN1CCC(c2c[nH]c3ccc(NC(=O)C4CCC4)nc23)CC1
Reaction #194771
DOI: 10.1039/C8SC04228D
Cc1cc(C(=O)Nc2cc(Oc3ccc4nc(NC(=O)C5CCC5)cn4n3)ccc2C)n(C)n1
Reaction #197557
DOI: 10.1039/C8SC04228D
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