formamide

CC(C)(C)OC(=O)N1CCN(c2ccc3oc(C(N)=O)cc3c2)CC1
Reaction #1266
5-(4-tert-butoxycarbonyl-1-piperazinyl)benzofuran-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1c2[nH]cnc2n(CC2CC2)c(=O)n1CC1CC1
Reaction #3739
1,3-Di-cyclopropylmethyl xanthine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1c(CCO)cc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #4852
2-(2-amino-3,5-dinitrophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)(C)c1cnc[nH]1
Reaction #7202
title compound
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc(-c2cnc[nH]2)c1
Reaction #7206
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1C[C@H](O)C[C@H]1C(=O)O
Reaction #10036
title compound
Выход 92.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Nc1ncnc2[nH]nc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #42903
4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(N)c1cccc(Br)c1
Reaction #45376
1-(3-bromophenyl)ethanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ncnc2[nH]nc(-c3ccc(Oc4ccccc4)cc3)c12
Reaction #46391
4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]cnc2ccc3c(c12)CCS3(=O)=O
Reaction #46394
desired compound
Выход 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1[nH]cnc2sc3c(c12)CCC3
Reaction #51063
3,5,6,7-Tetrahydro-4H-cyclopenta[4,5]thieno[2,3-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cl.NC1CCCCc2sccc21
Reaction #54646
5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-4-amine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(C)(C)OC(=O)C(C(=O)NC1C(=O)N2C(C(=O)O)=C(C(CC(=O)O)Sc3nnn[nH]3)CS[C@H]12)c1cccs1
Reaction #55416
7-(α-t-butoxycarbonylthienylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55955
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)c1ccc(N=Nc2ccc([N+](=O)[O-])cc2C#N)cc1
Reaction #55956
2-Cyano-4-nitro-4'-(N,N-diethylamino)azobenzene
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55957
2-cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Выход 83.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55958
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCN(CC)c1ccc(N=Nc2c(C#N)cc([N+](=O)[O-])cc2[N+](=O)[O-])c(NC(C)=O)c1
Reaction #55959
2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=c1ncnc2ccc3c[nH][nH]c3c12
Reaction #56044
formula 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=c1ncnc2cc3[nH][nH]cc3cc12
Reaction #56047
1H-Pyrazolo[4,5-g]-quinazoline-5-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
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