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238979

CCc1cncc(-c2cc3c(cn2)cnn3-c2cccc(N3CCNCC3)n2)c1
Reaction #86088
solid
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2cccc(N3CCNCC(O)C3)n2)c1
Reaction #86089
solid
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cncc(-c2cc3c(cn2)cnn3-c2cccc(F)n2)c1
Reaction #86091
1-(6-fluoro-2-pyridyl)-6-(5-isopropenyl-3-pyridyl)pyrazolo[4,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cncc(-c2cc3c(cn2)cnn3-c2cccc(F)n2)c1
Reaction #86092
1-(6-fluoropyridin-2-yl)-6-(5-isopropylpyridin-3-yl)-1H-pyrazolo[4,3-c]pyridine
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cncc(-c2cc3c(cn2)cnn3-c2cccc(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)c1
Reaction #86093
tert-butyl N-[(3S)-1-[6-[6-(5-isopropyl-3-pyridyl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cncc(-c2cc3c(cn2)cnn3-c2cccc(N3CCC[C@H](N)C3)n2)c1
Reaction #86094
108
Выход 37.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCNCC2)nc(-n2ncc3cnc(-c4cncc(C5CC5)c4)cc32)c1
Reaction #86097
solid
Выход 31.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCNCC2)nc(-n2ncc3cnc(-c4cncc(C5CC5)c4)cc32)c1
Reaction #86098
solid
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2cccc(-n3ncc4cnc(-c5cncc(C6COC6)c5)cc43)n2)CCN1
Reaction #86099
solid
Выход 24.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCNCC2)nc(-n2ncc3cnc(-c4cncc(C5COC5)c4)cc32)c1
Reaction #86100
solid
Выход 13.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1CNCCN(c2cccc(-n3ncc4cnc(-c5cncc(C6CC6)c5)cc43)n2)C1
Reaction #86101
solid
Выход 17.0%DOI: 10.6084/m9.figshare.5104873.v1
OC1CNCCN(c2cccc(-n3ncc4cnc(-c5cncc(C6COC6)c5)cc43)n2)C1
Reaction #86102
solid
Выход 6.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3COCC[Si](C)(C)C)c1
Reaction #86105
2-[[6-(5-ethyl-3-pyridyl)pyrazolo[4,3-c]pyridin-1-yl]methoxy]ethyl-trimethyl-silane
Выход 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3[nH]ncc3cn2)c1
Reaction #86106
6-(5-ethyl-3-pyridyl)-1H-pyrazolo[4,3-c]pyridine
Выход 174.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(Cl)c(F)n2)c1
Reaction #86107
1-(5-chloro-6-fluoro-2-pyridyl)-6-(5-ethyl-3-pyridyl)pyrazolo[4,3-c]pyridine
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(Cl)c(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)c1
Reaction #86108
tert-butyl N-[(3S)-1-[3-chloro-6-[6-(5-ethyl-3-pyridyl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamate
Выход 80.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(Cl)c(N3CCC[C@H](N)C3)n2)c1
Reaction #86109
117
Выход 36.2%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(N2CCCNCC2)nc(-n2ncc3cnc(-c4cncc(C5COC5)c4)cc32)c1
Reaction #86110
solid
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(C3CC3)c(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)c1
Reaction #86114
tert-butyl N-[(3S)-1-[3-cyclopropyl-6-[6-(5-ethyl-3-pyridyl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]-3-piperidyl]carbamate
Выход 248.6%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cncc(-c2cc3c(cn2)cnn3-c2ccc(C3CC3)c(N3CCC[C@H](N)C3)n2)c1
Reaction #86115
139
Выход 7.4%DOI: 10.6084/m9.figshare.5104873.v1