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602252

CCOC(=O)C(N=[N+]=[N-])C(O)c1cccnc1Cl
Reaction #83798
title compound
Выход 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N=[N+]=[N-])C(O[Si](C)(C)C(C)(C)C)c1cccnc1Cl
Reaction #83799
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)C(O[Si](C)(C)C(C)(C)C)c1cccnc1Cl
Reaction #83800
title compound
Выход 113.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2c(C(O)c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3)ncc21
Reaction #88433
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-(4-chlorophenyl)-5-((4-chlorophenyl)(hydroxy)methyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 20.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(O)c1c(Cl)ncc2c1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)n2C
Reaction #88435
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 32.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(O)c1c(-c2ccc(Cl)cc2)ncc2c1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)n2C
Reaction #88436
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-(4-chlorophenyl)-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2c(C(O)c3ccc(Cl)cc3)c(Cl)ncc21
Reaction #88440
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-((4-chlorophenyl)(hydroxy)methyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 30.0%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
Выход 13.0%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
Выход 14.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2cc(Oc3cccc(Cl)c3)ncc21
Reaction #88446
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-(3-chlorophenoxy)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(O)c1c(-c2cccc(Cl)c2)ncc2c1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)n2C
Reaction #88449
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-(3-chlorophenyl)-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2c(C(O)c3ccccc3)c(Cl)ncc21
Reaction #88453
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-(hydroxy(phenyl)methyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H, 3H)-dione
Выход 30.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2c(C(O)c3ccccc3)c(-c3cccc(OC(F)(F)F)c3)ncc21
Reaction #88454
3-(3-(tert-butyldimethylsilyloxy)propyl)-5-(hydroxyl(phenyl)methyl)-1-methyl-6-(3-(trifluoromethoxy)phenyl)pyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cccnc1Cl
Reaction #90352
1-(2-chloropyridin-3-yl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1n[nH]c2ncc(Br)cc12
Reaction #90353
methyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cccnc1Cl
Reaction #90356
1-(2-chloropyridin-3-yl)ethanol
Выход 38.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccnc1Cl
Reaction #90357
1-(2-chloropyridin-3-yl)ethanone
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(O)c2cccnc2Cl)c1
Reaction #93813
title product
Выход 59.8%DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccccc1)c1cccnc1Cl
Reaction #93814
product
Выход 42.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(c1ccccc1)c1cccnc1Cl
Reaction #93817
2-chloro-α-phenyl-3-pyridinemethanol acetate
DOI: 10.6084/m9.figshare.5104873.v1
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