N,N-dimethylethanamine

—
Reaction #55037
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC[NH+](C)C.O=S(=O)([O-])C(F)(F)F
Reaction #70117
dimethylethylammonium trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)CCOc1ccc(N2CCN(Cc3cc4cnc(C#N)nc4n3CC(C)(C)C)CC2)cc1
Reaction #202197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(N2CCOCC2)nc1)N1CCC(c2ncnc3cc(OCCCn4cnnc4)ccc23)CC1
Reaction #264526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(C)CCOc1ccc(N2CCN(Cc3cc4cnc(C#N)nc4n3CC(C)(C)C)CC2)cc1
Reaction #358756
6-{4-[4-(2-dimethylamino-ethoxy)-phenyl]-piperazin-1-ylmethyl}-7-(2,2-dimethyl-propyl)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C1OC(CO)CC1Cc1c(Cl)cc(-c2ccc(C(=O)N3CCC(C(F)(F)F)CC3)cc2)cc1Cl
Reaction #368244
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=CCN1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(Br)cs2)C1
Reaction #425304
title compound
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
O=C(NC1=N[C@@]2(c3ccccc3)CN(C(=O)OCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #425311
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC[N+](C)(C)COC.[Cl-]
Reaction #470362
N-ethyl-N-methoxymethyl-N,N-dimethylammonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC[N+](C)(C)COC.[Cl-]
Reaction #490254
N-ethyl-N-methoxymethyl-N,N-dimethylammonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCCOC(=O)C(CC1CCCC1=O)NC(C)=O
Reaction #511521
propyl 2-acetamido-3-(2-oxocyclopentyl)propanoate
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=CCN1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(Br)cs2)C1
Reaction #557427
title compound
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(NC1=N[C@@]2(c3ccccc3)CN(C(=O)OCc3ccccc3)C[C@H]2CS1)c1ccccc1
Reaction #557434
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CN(C)CC[CH2][AlH][CH2]CCN(C)C
Reaction #576891
AlH(CH2CH2CH2NMe2)2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
CC[N+](C)(C)COC.[Cl-]
Reaction #730369
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC[NH+](C)C.O=S(=O)([O-])C(F)(F)F
Reaction #742271
Dimethylethylammonium Trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCN(C)C
Reaction #744433
DMEA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCCOC(=O)C(CC1CCCC1=O)NC(C)=O
Reaction #757551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1OCCN1c1cc(Br)cs1
Reaction #903092
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COc1ccc(NC(C)=O)c(C)c1
Reaction #942974
colorless crystals
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
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