N,N-dimethylcarbamyl chloride

CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #921
title compound
Rendimiento 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)Nc1cc(Br)ccc1N1CCc2ccccc21
Reaction #4117
product
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN(C)C(=O)Nc1cc(Br)ccc1N1CCc2ccccc21
Reaction #4175
product
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)c1c(NC(=O)N(C)C)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc2n(C)c1=O
Reaction #42087
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC1CC2(CC(COC(=O)N(C)C)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44024
112
Rendimiento 136.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C(=O)OCC1c2cn[nH]c2CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44043
(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl dimethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C(=O)N[C@H]1CC[C@H](CCN2CCN(c3cccc(Cl)c3Cl)CC2)CC1
Reaction #44398
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C(=O)Oc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49458
4-dimethylcarbamoyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Rendimiento 99.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)C(=O)C#C[C@H]1CC[C@H](N(C)C(=O)OC(C)(C)C)CC1
Reaction #53863
trans-(4-Dimethylcarbamoylethynyl-cyclohexyl)-methyl-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)C(=O)n1cnc(C#N)c1C#N
Reaction #55310
1-(N,N-Dimethylcarbamoyl)-4,5-dicyanoimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CSc1cc(C)c(OC(=O)N(C)C)cc1C
Reaction #55613
4-dimethylcarbamoyloxy-2,5-dimethylphenyl methyl sulphide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Cc1ccc(S(=O)(=O)n2ccc3c(-c4oc(C)nc4-c4ccc(NC(=O)N(C)C)cc4)ccnc32)cc1
Reaction #57223
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C)C(=O)OC(c1ccccc1)c1nc(-c2ccccc2)c(-c2nc3c(N)ncnc3s2)n1C
Reaction #60895
title compound
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C)C(=O)Nc1cc(Br)ccc1N1CCc2ccccc21
Reaction #62647
product
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CN(C)C(=O)Nc1cc(Br)ccc1N1CCc2ccccc21
Reaction #63403
product
Rendimiento 40.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCOC(=O)C1=CN(C(=O)c2ccc(F)cc2)CC(C)(C)c2c1[nH]c1cc(OC(=O)N(C)C)ccc21
Reaction #66233
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC(=O)N(C)C)cc2n1Cc1ccccc1
Reaction #68326
title compound
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)C(=O)OCc1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1
Reaction #70471
title compound
Rendimiento 27.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)C(=O)Nc1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)CC2)nc1
Reaction #70494
title compound
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)C(=O)NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3cccc(C(F)(F)F)c3)c2)ncn1
Reaction #73345
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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