methylamine

CNc1cncc(C(F)(F)F)c1
Reaction #277
Выход 0.0%750 AstraZeneca ELN dataset
CNc1nc2ccc([N+](=O)[O-])cc2s1
Reaction #394
Выход 6.2%750 AstraZeneca ELN dataset
CNc1ccncc1[N+](=O)[O-]
Reaction #1008
4-methylamino-3-nitropyridine
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNCc1cc(Cl)c(F)cn1
Reaction #1962
title compound
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2317
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNCc1ccc(C(=O)Nc2ccccc2OC)cc1
Reaction #2551
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNCCC#Cc1cccnc1
Reaction #2816
XIII
Выход 546.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1cnc(SC)nc1NC
Reaction #3264
4-methylamino-2-methylsulfanyl-5-pyrimidinecarboxylate ethyl ester
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(C)c2n1
Reaction #3278
pure product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1nc2nc(N)ncc2cc1-c1ccc(OC)cc1
Reaction #3510
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNS(=O)(=O)c1cc(-c2nc3nc(OC)ncc3[nH]2)c(OC)cc1Cl
Reaction #3975
2-Methoxy-8-(2-methoxy-4-chloro-5-methylaminosulfonyl-phenyl)-purine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNS(=O)(=O)c1ccc(-c2nc3c[nH][nH]c(=O)c-3n2)c(OC)c1
Reaction #3980
2-(2-Methoxy-4-methylaminosulfonyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNCCS(=O)(=O)c1ccccc1
Reaction #4297
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNC(=O)OC(Cl)C(Cl)(Cl)Cl
Reaction #4526
1,2,2,2-tetrachloroethyl N-methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNc1c(CC(C)O)cc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #4855
1-(2-methylamino-3,5-dinitrophenyl)-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1C(=O)C[C@H](O)C1=O
Reaction #4889
(S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNCC(O)CN(C)C.Cl
Reaction #4950
1-dimethylamino-3-methylamino-2-propanol hydrochloride
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CNC[C@H]1O[C@@H](n2cc(C)c(=O)[nH]c2=O)C[C@@H]1O
Reaction #4987
5'-Deoxy-5'-(methyl-amino)-thymidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #5167
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNC(=O)c1ccnc(NCCCN2CCN(c3cccc(Cl)c3)CC2)n1.Cl
Reaction #5436
base
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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