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19262

O=C(C1CC12CCN(c1ccccn1)CC2)N1CCN(C2CCC2)CC1
Reaction #827
Выход 26.6%
O=C(C1CC12CCN(c1ccccn1)CC2)N1CCN(C2CCC2)CC1
Reaction #828
Выход 9.4%
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC1C)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7647
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]-2-methylcyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)C1CC1)c1nnc(C2CCCC2)[nH]c1=O
Reaction #7648
N-[1-(3-Cyclopentyl-5-oxo-4,5-dihydro-1,2,4-triazin-6-yl)propyl]cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc(C2CC2C)n2nc(C3CCCC3)[nH]c(=O)c12
Reaction #7670
2-Cyclopentyl-5-ethyl-7-(2-methylcyclopropyl)imidazo[5,1-f][1,2,4]triazin-4(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(CNC(=O)C2CC2)c1C(=O)OC
Reaction #10049
product
Выход 103.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)C4CC4)c3C2=O)C(=O)N1
Reaction #10102
cyclopropanecarboxylic acid [2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-amide
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2Cc3c(CNC(=O)C4CC4)cccc3C2=O)C(=O)N1
Reaction #10161
N-{[2-(2,6-dioxo(3-piperidyl))-1-oxoisoindolin-4-yl]methyl}cyclopropylcarboxamide
Выход 50.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1CC1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41283
N-((1S,2R)-2-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-methyl-2-phenylethyl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1(C)CC1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccc2c(c1)OCCO2
Reaction #41431
N-((1R,2S)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)propan-2-yl)-1-methylcyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1(O)CC1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccc(C(F)(F)F)cc1
Reaction #41451
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-[4-(trifluoromethyl)phenyl]propan-2-yl]-1-hydroxy-cyclopropane-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)C5CC5)c4)CC3)cccc2n1
Reaction #44076
title compound
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(NC(=O)C2CC2)c(OC(=O)C2CC2)c(Br)c1-c1ccccc1
Reaction #45582
2-bromo-5-cyano-4-(cyclopropanecarbonylamino)-6-methylbiphenyl-3-yl cyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1c(N)c(C#N)c(C)c(Br)c1F
Reaction #45606
compound
Выход 97.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #46086
solid
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(c2ccc3c(c2)OCO3)CC1
Reaction #46176
solid
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(OC)c(CCl)c2)CC1
Reaction #46187
1-(3-chloromethyl-4-methoxy-phenyl)-cyclopropanecarboxylic acid methyl ester
Выход 102.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(OC)c(CO)c2)CC1
Reaction #46188
1-(3-hydroxymethyl-4-methoxy-phenyl)-cyclopropanecarboxylic acid methyl ester
Выход 43.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Br)cn1)C1(c2ccc3c(c2)OCO3)CC1
Reaction #46228
product
Выход 83.3%DOI: 10.6084/m9.figshare.5104873.v1
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