Recherche de Sous-structure

1250459

C[Si](C)(C)CCOCn1nc(-c2ccnc(C3CC3)n2)cc(-c2nc3ccccc3n2COCC[Si](C)(C)C)c1=O
Reaction #40574
6-(2-Cyclopropylpyrimidin-4-yl)-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc([C@@H]3C[C@H]3c3ccccc3)cc2c(N2CCOCC2)c1S(C)(=O)=O
Reaction #41938
white crystals
Rendement 61.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc(C3CC3)cc2c(N2CCOCC2)c1S(C)(=O)=O
Reaction #41944
white crystals
Rendement 22.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CC(C)C)N1CC(Oc2cccc(C3CC3)c2F)=CC1=O
Reaction #47445
(S)-2-[4-(3-cyclopropyl-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid ethyl ester
Rendement 710.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(C2CC2)c1
Reaction #48069
3-cyclopropyl-4-fluorophenylamine
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(C3CC3)c3c2C(=O)NC3)cc2cc(CN3CCN(CCO[Si](C)(C)C(C)(C)C)CC3)ccc21
Reaction #49500
4-cyclopropyl-7-{1-(tert-butoxycarbonyl)-5-[4-(2-tert-butyldimethylsilyloxyethyl)pyperazin-1-ylmethyl]indol-2-yl}isoindolinone
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(F)(F)F)cc1C1CC1
Reaction #67702
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ncc(C2CC2)cn1
Reaction #68842
2-Chloro-5-cyclopropylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc([N+](=O)[O-])cc1-c1ccccc1
Reaction #70260
2-methoxy-5-nitro-3-phenylpyridine
Rendement 60.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc(C2CC2)c(-c2ccccc2)c1
Reaction #70267
2-cyclopropyl-5-nitro-3-phenylpyridine
Rendement 17.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1N
Reaction #70276
expected product
Rendement 88.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C2CC2)ccc1Cl
Reaction #70277
expected product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ncc(N)cc2C2CC2)c1
Reaction #70304
5-Cyclopropyl-6-(3-methoxyphenyl)pyridin-3-amine
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1N
Reaction #70315
expected product
Rendement 88.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(-c2ccccc2C2CC2)nc1
Reaction #70340
5-Cyclopropyl-2-(2-(2-cyclopropylphenyl)pyrimidin-5-ylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3C3CC3)c(C)c2)c(C(=O)OC(C)(C)C)c1
Reaction #70345
tert-Butyl 2-(6-(2-cyclopropylphenyl)-5-methylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc2c1ccn2C1CC1
Reaction #70789
methyl 6-bromo-1-cyclopropyl-1H-indole-4-carboxylate
Rendement 71.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1S(=O)(=O)N1CCN(C(=O)c2ccc(C3CC3)nc2)[C@@H](C)C1
Reaction #71707
title compound
Rendement 2.4%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCCNCC2)nc(-n2ncc3cnc(-c4cnn(C5CC5)c4)cc32)c1
Reaction #86158
solid
Rendement 25.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(-c2nc(C(F)F)c(C3CC3)s2)cnn1C
Reaction #88422
title compound
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant