Substructure Search

1216831

O=C(O)c1cn(C2CC2)c2nc(N3CCC(c4ccccn4)C3)c(F)cc2c1=O
Reaction #82758
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2cccc(-n3ncc4cnc(Cl)cc43)n2)CC1
Reaction #86139
tert-butyl 4-[6-(6-chloropyrazolo[4,3-c]pyridin-1-yl)-2-pyridyl]-3,6-dihydro-2H-pyridine-1-carboxylate
Yield 92.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cccc(C3=CCN(C(=O)OC(C)(C)C)CC3)n2)n1
Reaction #86140
desired product
Yield 72.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cccc(C3CCN(C(=O)OC(C)(C)C)CC3)n2)n1
Reaction #86153
tert-butyl 4-[6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-2-pyridyl]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cccc(C3CCNCC3)n2)n1
Reaction #86154
166
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(C3(O)CCCNCC3)n2)cn1
Reaction #86222
230
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(O)(c2cccc(-n3ncc4cnc(Cl)cc43)n2)CC1
Reaction #86228
tert-butyl 4-(6-(6-chloro-1H-pyrazolo[4,3-c]pyridin-1-yl)pyridin-2-yl)-4-hydroxyazepane-1-carboxylate
Yield 63.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(C3(O)CCCN(C(=O)OC(C)(C)C)CC3)n2)cn1
Reaction #86229
tert-butyl 4-hydroxy-4-(6-(6-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[4,3-c]pyridin-1-yl)pyridin-2-yl)azepane-1-carboxylate
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc3c(cn2)cnn3-c2cccc(C3(F)CCCNCC3)n2)cn1
Reaction #86230
1-(6-(4-fluoroazepan-4-yl)pyridin-2-yl)-6-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[4,3-c]pyridine
Yield 110.7%DOI: 10.6084/m9.figshare.5104873.v1
NCC[C@@H](O)c1cccc(OCC2CCN(C(=O)OCc3ccccc3)CC2)n1
Reaction #91623
(R)-benzyl 4-(((6-(3-amino-1-hydroxypropyl)pyridin-2-yl)oxy)methyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #157865
( A )
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #157876
crude product
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc([C@]2(CCN3Cc4ccsc4C3)CCOC3(CCCC3)C2)nc1
Reaction #163410
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H]2CN(S(=O)(=O)c3ccc(Cl)c(Cl)c3)Cc3cccnc3[C@@H]2C1
Reaction #172149
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc2c(c1)CC1(C2)C(=O)N(COCC[Si](C)(C)C)c2ncc(F)cc21
Reaction #178516
DOI: 10.1039/C8SC04228D
COc1ccc(C2CC(c3ccccn3)Nc3c(Br)c(-c4ccccc4)nn32)cc1OC
Reaction #183385
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CNc1cc(Cl)cnc12
Reaction #187733
DOI: 10.1039/C8SC04228D
CC(C)C(=O)Nc1cccc(C2CCN(CCCNC(=O)C3(c4ccc(F)cc4)CCCC3)CC2)n1
Reaction #187881
DOI: 10.1039/C8SC04228D
CCC1CC(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(C)=O)c2nc(N(C)C)ccc2N1C(=O)OC(C)C
Reaction #212371
DOI: 10.1039/C8SC04228D
Cl.O=C(CCc1ccccn1)NNC(=O)N1Cc2ccccc2Oc2ccc(Cl)cc21
Reaction #215828
white powder
Yield 153.4%DOI: 10.6084/m9.figshare.5104873.v1
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