N,N-dimethylacrylamide

COc1cc(-c2csc3c(C(=O)NC4CCCN(CCC(=O)N(C)C)C4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45461
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(-c2csc3c(C(=O)NC4CCCN(CCC(=O)N(C)C)C4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45488
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(/C=C/C(=O)N(C)C)ccc3OCC)nc12
Reaction #50209
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #157534
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #157545
solid
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C1CCOC1=O.C=CC(=O)N(C)C
Reaction #171132
α-methylene-γ-butyrolactone N,N-dimethyl acrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #172805
solid
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(CC)CCC(=O)N(C)C
Reaction #195825
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(C=CC(=O)N(C)C)cc(C)c1N(Cc1cccnc1)S(=O)(=O)c1ccc(OC)cc1
Reaction #247553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(OCCC(=O)N(C)C)C1=CCC2C3=CC=C4CC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C4(C)C3CCC12C
Reaction #284535
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cc(-c2csc3c(C(=O)NC4CCCN(CCC(=O)N(C)C)C4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #301197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCNC(=O)Nc1cn2ccc(-c3nc(C)n(C)n3)cc2n1
Reaction #316550
pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CN(C)C(=O)/C=C/c1ccc(-c2ccc([N+](=O)[O-])cc2)c2c(N)n[nH]c12
Reaction #327059
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCc1nc2cnc3cc(C=CC(=O)N(C)C)ccc3c2n1CC(C)(C)O
Reaction #332018
3-[2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylprop-2-enamide
المردود 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COCCc1nc2cnc3ccc(C=CC(=O)N(C)C)cc3c2n1CCCN1CCCC1=O
Reaction #332022
3-{2-(2-methoxyethyl)-1-[3-(2-oxopyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylprop-2-enamide
المردود 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCc1nc2c(N)nc3cc(/C=C/C(=O)N(C)C)ccc3c2n1CC1CCOCC1
Reaction #332063
(2E)-3-[4-amino-2-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylprop-2-enamide
المردود 63.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCCc1nn(C)c2c(=O)[nH]c(-c3cc(C=CC(=O)N(C)C)ccc3OCC)nc12
Reaction #389711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCc1nn(C)c2c1N=C(c1cc(/C=C/C(=O)N(C)C)ccc1OCC)NC2
Reaction #414229
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #419326
title compound
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CN(C)C(=O)CCSc1ccc(Cl)cc1N
Reaction #419337
solid
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
الصفحة 1التالي