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CNCC(F)F.Cl

CC(C)(C)[C@@H]1N(c2cc(Cl)cc(Cl)c2)C(=O)[C@@](C)(Cc2ccc(OC(F)(F)F)cc2)N1C(=O)C(F)(F)F
Reaction #52115
(2R,5R)-2-tert-butyl-3-(3,5-dichloro-phenyl)-5-methyl-1-(2,2,2-trifluoro-acetyl)-5-(4-trifluoromethoxy-benzyl)-imidazolidin-4-one
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3nc(CNCC(F)(F)F)c[nH]3)c3nccnc23)c1Cl
Reaction #71499
title compound
Выход 62.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F)C(F)(F)F
Reaction #87661
desired product
Выход 46.3%DOI: 10.6084/m9.figshare.5104873.v1
NCc1cc(-c2nn(-c3ccc(F)c(Cl)c3)c(=O)[nH]2)c(Cl)cc1F
Reaction #87662
desired product
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(-n2nc(-c3ccc(I)cc3)[nH]c2=O)c(Cl)cc1F)C(F)(F)F
Reaction #87667
desired product
Выход 61.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)N(C(=O)C(F)(F)F)CCO2)c1cc(Br)ccc1Cl
Reaction #159747
1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Выход 79.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCOc2ccc(Cc3cc(Br)ccc3Cl)cc21)C(F)(F)F
Reaction #159748
1-[6-(5-bromo-2-chloro-benzyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Выход 61.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Br)cc1Cc1ccc2c(c1)NCCO2
Reaction #159749
6-(5-bromo-2-chloro-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc2c(c1)N(C(=O)C(F)(F)F)CCO2)c1cc(Br)ccc1Cl
Reaction #159753
1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCOc2ccc(Cc3cc(Br)ccc3Cl)cc21)C(F)(F)F
Reaction #159754
1-[6-(5-bromo-2-chloro-benzyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone
Выход 85.9%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Br)cc1Cc1ccc2c(c1)NCCO2
Reaction #159755
6-(5-bromo-2-chloro-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn[nH]c1C1CN(CC(F)F)CC2(CCNCC2)O1
Reaction #160066
8-(2,2-difluoroethyl)-10-(4-methyl-1H-pyrazol-5-yl)-11-oxa-3,8-diazaspiro[5.5]undecane
DOI: 10.6084/m9.figshare.5104873.v1
Cl.FC1(F)CC[C@H]2OCCN[C@@H]21
Reaction #168337
trans-5,5-difluorooctahydrocyclopenta[b][1,4]oxazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C(=O)C(F)(F)F)CCc2cc(O)c(Cl)cc21
Reaction #171273
white solid
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1cc2c(cc1Cl)C(C)CN(C(=O)C(F)(F)F)CC2
Reaction #171274
white solid
Выход 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C(=O)C(F)(F)F)CCc2cc(F)c(Cl)cc21
Reaction #171307
white solid
Выход 60.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1CNCCc2cc(F)c(Cl)cc21
Reaction #171308
clear oil
Выход 197.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C=Cc2ccnc(Cl)n2)c1)C(F)(F)F
Reaction #179073
DOI: 10.1039/C8SC04228D
N#Cc1c(Oc2cc(NC(=O)C(F)(F)F)c(F)cc2Cl)ccc2nc(NC(=O)C3CC3)sc12
Reaction #185657
DOI: 10.1039/C8SC04228D
COc1ccc(NC(Cc2ccc(Cl)cc2CNC(=O)C2CCCN2C(=O)OC(C)(C)C)C(F)F)cc1
Reaction #194978
DOI: 10.1039/C8SC04228D
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