dimethylamine hydrochloride

C#CCn1c(-c2ccccc2)nc(C(=O)N(C)C)c(C)c1=O
Reaction #1548
6-dimethylaminocarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)c1cc(CCl)nc(N)n1
Reaction #4006
2-amino-4-chloromethyl-6-dimethylaminopyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCC(CCc1cc(OC)ccc1I)N(C)C.Cl
Reaction #4381
2-Iodo-5-methoxy-N,N-dimethylalphapentylbenzenepropanamine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN(C)CC1CCc2c(c3cc(Br)ccc3n2C)C1=O.Cl
Reaction #4474
solid
Ausbeute 67.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN(C)CC1CCc2c(c3cc(C(N)=O)ccc3n2C)C1=O
Reaction #4481
3-[(Dimethylamino)methyl]-2,3,4,9-tetrahydro-9-methyl-4-oxo-1H-carbazole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN(C)CC1=NC=C(OCc2ccccc2)C(=O)C1
Reaction #5608
5-benzyloxy-2-(N,N-dimethylamino)methyl-4-pyridone
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C)CC1CCCCC1=O
Reaction #40765
light-yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCC(=O)c1ccccc1.Cl
Reaction #40768
white crystalline material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCC(=O)c1ccc(Cl)cc1.Cl
Reaction #40770
product
Ausbeute 112.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1c(C(=O)N(C)C)c(=O)n(C)c2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
Reaction #42128
4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-N,N,1-trimethyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)Cc1cc(C#N)ccn1
Reaction #42557
4-cyano-2-(dimethylamino)methylpyridine
Ausbeute 66.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)c1ccc2nc3ccc(N(C)C)cc3[s+]c2c1.[I-]
Reaction #42645
3-(N,N-dimethylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H]1CC[C@H](C(=O)N(C)C)CC1
Reaction #44989
methyl trans-4-[(dimethylamino)carbonyl]-cyclohexanecarboxylate
Ausbeute 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(F)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45650
compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(Br)c(F)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45671
compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2cccc(Cl)c2)c(F)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45878
compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(CC(=O)N(C)C)c2oc(C3CC3)nc2c1C#N
Reaction #45883
compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C[C@@H]1CCCN1C(=O)OC(C)(C)C
Reaction #45898
compound
Ausbeute 4.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C1(C#N)CCCC1
Reaction #49061
title product
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C1(C#N)CCCC1
Reaction #49062
title product
Ausbeute 96.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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