部分構造検索

1339049

OCCN1CCN(c2ccccc2F)CC1
Reaction #77309
title compound
収率 65.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1N1CCN(CCCl)CC1
Reaction #77310
desired product
収率 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1CCN(c2ccc([N+](=O)[O-])cc2F)CC1=O
Reaction #187211
DOI: 10.1039/C8SC04228D
COCCN1CCN(c2ccc(N)cc2F)CC1=O
Reaction #188211
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)OC)c3ccccc3)CC2)c(F)c1
Reaction #197850
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)N1CCN(c2ccc(N3CC(COc4ccon4)OC3=O)cc2F)CC1
Reaction #198376
DOI: 10.1039/C8SC04228D
O=C(O)c1cn(C2CC2)c2nc3cc(N4CCN(CCO)CC4)c(F)cc3cc2c1=O
Reaction #223488
DOI: 10.1039/C8SC04228D
O=C(CO)N1CCN(c2ccc(C3=NOC(COc4ccon4)C3)cc2F)CC1
Reaction #227589
DOI: 10.1039/C8SC04228D
Fc1ccccc1N1CCN(CCCl)CC1
Reaction #245471
DOI: 10.1039/C8SC04228D
NC(=O)C1CN(c2ccc(N3CCN(C(=O)CO)CC3)c(F)c2)C(=O)O1
Reaction #266893
DOI: 10.1039/C8SC04228D
COc1c(N2CCN(CCOCCO)CC2)c(F)cc2c(=O)c(C(=O)NCc3ccc(Cl)cc3Cl)cn([C@@H]3C[C@@H]3F)c12
Reaction #339041
target compound
収率 59.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CC(C)N(CC(C)(C)O)C(C)C2)c(F)cc2c(=O)c(C(=O)NCc3ccc(Cl)cc3Cl)cn(C3CC3)c12.Cl
Reaction #339044
1-Cyclopropyl-N-(2,4-dichlorobenzyl)-7-[(3RS,5SR)-3,5-dimethyl-4-(2-hydroxy-2-methylpropyl)piperazin-1-yl]-6-fluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CC(C)N(C[C@@H](O)CO)C(C)C2)c(F)cc2c(=O)c(C(=O)NCc3ccc(Cl)cc3Cl)cn(C3CC3)c12.Cl
Reaction #339045
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2cc(F)c(N3CCN(C(=O)CO)CC3)c(F)c2)C(=O)O1
Reaction #353895
(S)-N-[[3-[3,5-difluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide
収率 98.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COCc1ccccc1
Reaction #353896
benzyloxyacetic acid
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)OCC(=O)N1CCN(c2ccc(N3CC(CNC(C)=O)OC3=O)cc2F)CC1
Reaction #353897
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCC(O)CN2CCN(c3ccccc3F)CC2)c2ccccc2c1OCc1ccccc1.Cl
Reaction #364815
white crystals
収率 57.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(C)=O)N1CCN(c2cc3c(cc2F)c(=O)c(C(=O)O)cn3C2CC2)CC1
Reaction #370783
DOI: 10.1039/C8SC04228D
CCC(CC)NC(=O)c1ccc(N2CCN(C(C(=O)OC)c3ccccc3)CC2)c(F)c1
Reaction #374119
DOI: 10.1039/C8SC04228D
COCCN1CCN(c2c(F)cc(N3CC(CNC(C)=O)OC3=O)cc2F)CC1
Reaction #375211
DOI: 10.1039/C8SC04228D
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