ethanol;hydrochloride

CN(C)c1cccc(NC(=O)N[C@@H]2N=C(c3ccccn3)c3ccccc3N(CC(=O)C(C)(C)C)C2=O)c1.Cl
Reaction #2436
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc(Cl)c(Cl)n1CCCCN1CC=C(c2ccccc2)CC1.Cl
Reaction #2888
4,5-dichloro-2-methyl-1-[4-(4-phenyl-1,2,3,6-tetrahydro-1-pyridyl)-butyl]-1H-imidazole hydrochloride
Выход 189.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(CC(=O)Nc2ccc3c(c2)C(=O)C(=Cc2ccccc2)CC3)ccc1O
Reaction #7180
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(-c2ccccc2)c(N2CC[C@H](N(C)C)C2)c2oc(CCc3ccccc3)nc2c1C#N
Reaction #45629
compound
Выход 16.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C=O)c(N2CC[C@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N.Cl
Reaction #45740
2-Cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-formyl-5-methyl-1,3-benzoxazole-4-carbonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C2C=CC=C2)c(N2CC[C@H](N(C)C)C2)c2oc(C3CC3)nc2c1C#N
Reaction #45872
compound
Выход 78839.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1ccc2[nH]c(C(=O)OCC)cc2c1
Reaction #51418
1H-indole-2,5-dicarboxylic acid diethyl ester
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #55744
2-allyloxy
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CN1CCC(C(=O)c2ccccn2)CC1.Cl.Cl
Reaction #58502
6-(1-methylpiperidin-4-ylcarbonyl)-pyridine 2HCl
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C1CNCCN1CCc1ccc2c(c1)OCCO2
Reaction #67962
ethyl 1-(2-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl)piperazine-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(S(=O)(=O)NC(C)(C)C)ccc1CN
Reaction #70618
4-(aminomethyl)-N-tert-butyl-3-methylbenzenesulfonamide
Выход 113.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)NS(=O)(=O)c1cc(CN)ccc1F
Reaction #70640
5-aminomethyl-N-tert-butyl-2-fluoro-benzenesulfonamide
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cl.O=S1(=O)CCN2c3c(cccc31)[C@@H]1CNCC[C@@H]12
Reaction #79314
title compound
Выход 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cl.OC1(Cc2ccc(F)cc2)CCNCC1
Reaction #88870
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.OC1(Cc2ccc(F)c(F)c2)CCNCC1
Reaction #88882
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.OC1(Cc2ccc(F)cc2F)CCNCC1
Reaction #88885
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CN(CCc3cccnc3)C(=O)c3ccccc3)ccc21.Cl
Reaction #156146
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl.Cl.Cn1c(=O)c(OCCCCCN(CCc2cccnc2)CC2CCCCC2)cc2ccccc21
Reaction #156185
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl.Cl.Cl.Cn1c(=O)ccc2cc(OCCN(CCc3cccnc3)Cc3cccnc3)ccc21
Reaction #156196
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(OCCCn3c(-c4ccccc4)nc4ccccc43)ccc21.Cl
Reaction #156238
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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