Substructure Search

441527

CC1CCC(NC(=O)OC(C)(C)C)CN1c1cccc(Br)n1
Reaction #86155
tert-butyl N-[1-(6-bromo-2-pyridyl)-6-methyl-3-piperidyl]carbamate
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cl)nc1N1C[C@@H](NC(=O)OC(C)(C)C)CCC1=O
Reaction #86201
desired product
Yield 55.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Br)nc(N2CCC[C@H](NC(=O)OC(C)(C)C)C2)c1=O
Reaction #86233
tert-butyl N-[(3S)-1-(6-bromo-4-methyl-3-oxo-pyrazin-2-yl)-3-piperidyl]carbamate
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc(-c2cc3c(cn2)cnn3-c2cn(C)c(=O)c(N3CCC[C@H](NC(=O)OC(C)(C)C)C3)n2)n1
Reaction #86234
tert-butyl N-[(3S)-1-[4-methyl-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-3-oxo-pyrazin-2-yl]-3-piperidyl]carbamate
Yield 70.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157010
tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157011
(R)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #157012
(S)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCN(c2ccccc2[N+](=O)[O-])C1
Reaction #157014
tert-butyl 1-(2-nitrophenyl)piperidin-3-ylcarbamate
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCCC(NC(=O)OC(C)(C)C)C2)c([N+](=O)[O-])c1
Reaction #157027
tert-butyl 1-(4-methoxy-2-nitrophenyl)piperidin-3-ylcarbamate
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCCC(NC(=O)OC(C)(C)C)C2)c([N+](=O)[O-])c1
Reaction #157034
tert-butyl 1-(4-methyl-2-nitrophenyl)piperidin-3-ylcarbamate
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCCN(c2ccc(C(F)(F)F)cc2[N+](=O)[O-])C1
Reaction #157035
tert-butyl 1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-ylcarbamate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CN(c2ccncc2NC(=O)c2nc(Br)ccc2N)CC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #157112
trans-(+/−)-tert-butyl 1-(3-(3-amino-6-bromo-picolinamido)pyridin-4-yl)-4-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CN(c2ccncc2NC(=O)c2nc(-c3c(F)cccc3F)ccc2N)CC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #157157
tert-butyl (3R,4R)-1-(3-(3-amino-6-(2,6-difluorophenyl)picolinamido)pyridin-4-yl)-4-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2c(F)cccc2F)nc1C(=O)Nc1cnccc1N1CC[C@@H](O)[C@H](N)C1
Reaction #157158
3-amino-N-(4-((3R,4R)-3-amino-4-hydroxy-piperidin-1-yl)pyridin-3-yl)-6-(2,6-difluorophenyl)picolinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1C[C@@H](O[Si](C)(C)C(C)(C)C)CN(c2ccncc2NC(=O)c2ccc(F)c(Br)n2)C1
Reaction #157175
tert-butyl (3S,5R)-1-(3-(6-bromo-5-fluoropicolinamido)pyridin-4-yl)-5-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(CC(=O)O)C1=O
Reaction #158925
(R)-(3-tert-butoxycarbonylamino-2-oxo-piperidin-1-yl)-acetic acid
Yield 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccncc2[N+](=O)[O-])C1
Reaction #160691
(S)-tert-butyl 1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CNC[C@@H](NC(=O)OC(C)(C)C)C1
Reaction #160725
cis-(+/−)-tert-butyl 5-methylpiperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CN(c2ccncc2NC(=O)c2csc(Br)n2)CC[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #160787
tert-butyl (3R,4R)-1-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)-4-(tert-butyldimethylsilyloxy)piperidin-3-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCCN(CC(=O)O)C1=O
Reaction #166879
(R)-(3-tert-butoxycarbonylamino-2-oxo-piperidin-1-yl)-acetic acid
Yield 95.1%DOI: 10.6084/m9.figshare.5104873.v1
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