N,N-diethylaniline

Clc1ncnc2c1CCN(Cc1ccccc1)C2
Reaction #8810
7-benzyl-4-chloro-5,6,7,8-tetrahydro-pyrido[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(CCCNC(=O)OCCCCCCl)OCC
Reaction #10281
(4,4-diethoxybutyl)carbamic acid 5-chloro-pentyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(-c2cnn3c(Cl)cc(C)nc23)c(Cl)c1
Reaction #10332
7-chloro-5-methyl-3-(2-chloro-4-methylphenyl)pyrazolo[1,5-a]pyrimidine
수율 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1cccc(-c2cc(Cl)nc(N)n2)c1
Reaction #44705
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1nnnc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=S)CCC#N)[C@H]2SC1
Reaction #54317
( a )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCN(CC)c1ccc(C(=O)c2c(Cl)c(Cl)c(Cl)c(Cl)c2C(=O)O)c(C)c1
Reaction #55304
2-(4-(diethylamino)benzoyl)-3,4,5,6-tetrachlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CO[C@@]1(NC(=O)[C@H](O)c2ccccc2)C(=O)N2C(C(=O)O)=C(C(CCC(=O)O)Sc3nnn[nH]3)CS[C@@H]21
Reaction #55420
7β-D-Mandelamido-7α-methoxy-3-[1-(2-carboxyethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OC(C)C=C2
Reaction #62731
title compound
수율 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CN(C)N1C(=O)c2ccccc2C1=O
Reaction #72711
desired product
수율 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=CC(=O)OCCCCCCOc1ccc(C(=O)O)cc1OCCCCCCOC(=O)C=C
Reaction #75430
3,4-di-(6-acryloyloxyhexyloxy)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCCCCCCCCCCCCCCC(=O)OC[C@H](CCOC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)Cn1cnc2c(Cl)nc(N)nc21
Reaction #76834
(R)-2-Amino-9-(2-stearoyloxymethyl-4-(N-tert-butoxycarbonyl-L-valyloxy)butyl)-6-chloropurine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(Cl)c1cccc(C(N)=O)c1
Reaction #88802
title compound
수율 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cn1cnc2nc(Cl)nc(Cl)c21
Reaction #159358
2,6 dichloro-7-methyl-7H-purine
수율 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1cc(C(O)CBr)ccc1OCc1ccccc1
Reaction #184943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)c1cc2c(c(C3=CCCCC3)c1C(=O)c1ccc(C(F)(F)F)cc1)C(O)CC(C)(C)O2
Reaction #186129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)c1ccc2c(c1O)C=CCO2
Reaction #187410
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)OCc1ccccc1
Reaction #189932
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCc1cc(Cl)n2nc(SC)c(S(=O)(=O)c3ccccc3)c2n1
Reaction #191374
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC1CCc2c3c(c(F)c(F)c2O1)OC(C1CCC(CCC)CC1)C=C3
Reaction #193516
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCc1cc(Cl)c2oc(Cc3ccc(OC)cc3)c(C)c2c1O
Reaction #194626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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