部分構造検索

79707

Cc1cc(-c2nc3ccccc3o2)ccc1-c1ccccn1
Reaction #7851
2-(3-methyl-4-pyridin-2-ylphenyl)-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccccn1
Reaction #42149
2-ortho-tolylpyridine
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1ccccn1
Reaction #42166
2-ortho-tolylpyridine
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)-c1c(C)c3ccc4c(c3c[n+]1CC2)OCO4.[Cl-]
Reaction #42865
dehydrocavidine
収率 24.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)-c1c(C)c3ccc4c(c3c[n+]1CC2)OCO4.[Cl-]
Reaction #42866
dehydrocavidine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cn1c(-c2ccc3nc(-c4cc(OC)ccc4-c4ccc(Cl)cc4)ccc3c2)c(C2CCCCC2)c2ccc(C(=O)OC)cc21
Reaction #67328
2-[2-(4′-Chloro-4-methoxy-biphenyl-2-yl)-quinolin-6-yl]-3-cyclohexyl-1-methoxycarbonylmethyl-1H-indole-6-carboxylic acid methyl ester
収率 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1c(-c2ccc(F)cc2)oc2cnc(-c3cc(C(=O)O)ccc3C)cc12
Reaction #72373
3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)furo[2,3-c]pyridin-5-yl)-4-methylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)c1ccccc1-c1ccc(C(F)(F)F)cn1
Reaction #80189
title compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1-c1ccc(C(F)(F)F)cn1
Reaction #80190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccccc1-c1ncc2c(c1C(O)c1ccc(Cl)cc1)c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)n2C
Reaction #88441
3-(3-(tert-butyldimethylsilyloxy)propyl)-5-((4-chlorophenyl)(hydroxy)methyl)-6-(2-isopropylphenyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
収率 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccccc1-c1ncc2c(c1Cc1ccc(Cl)cc1)c(=O)n(CCCOC=O)c(=O)n2C
Reaction #88442
3-(5-(4-chlorobenzyl)-6-(2-isopropylphenyl)-1-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formate
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccccc1-c1ncc2c(c1Cc1ccc(Cl)cc1)c(=O)n(CCCO)c(=O)n2C
Reaction #88443
5-(4-chlorobenzyl)-3-(3-hydroxypropyl)-6-(2-isopropylphenyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
収率 36.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(O)c1c(-c2ccccc2C(C)C)ncc2c1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)n2C
Reaction #88444
3-(3-(tert-butyldimethylsilyloxy)propyl)-5-(1-hydroxy-3-methylbutyl)-6-(2-isopropylphenyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
収率 14.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCc1c(-c2ccccc2C(C)C)ncc2c1c(=O)n(CCCO)c(=O)n2C
Reaction #88445
3-(3-hydroxypropyl)-5-isopentyl-6-(2-isopropylphenyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
収率 23.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CN)c1
Reaction #89256
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(F)cn2)c1
Reaction #89257
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC[C@@H]2[C@H](C)CCCN2C(=O)c2cc(C)ccc2-c2ccccn2)nc1
Reaction #89258
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C#N)cn2)c1
Reaction #89259
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(Cl)cn2)c1
Reaction #89319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2nc3cc(F)ccc3o2)c1
Reaction #89330
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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