ammonium chloride

CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #921
title compound
収率 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccncc1NC(=O)c1c[nH]c2c1C(=O)CCC2
Reaction #1006
N-(4-methoxy-3-pyridyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole 3-carboxamide
収率 19.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CBr)NC1CCCOc2ccccc21
Reaction #1049
compound ( 8 )
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(OCCOc2ccc(C(C)(C)C)cc2)ccnc1C
Reaction #1113
2-Methyl-3-methoxy-4-[2-(4-tert-butylphenoxy)ethoxy]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nccc(NC2CCC(=Cc3ccc(Cl)cc3Cl)CC2)c1Cl
Reaction #1116
3-Chloro-4-[4-(2,4-dichlorobenzylidene)cyclohexyl]amino-2-ethylpyridine
収率 7.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Clc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1123
2-Chloro-3-bromo-4-(cis-4-phenylcyclohexylamino)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCc3nnn[nH]3)oc2c1
Reaction #1144
5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole
収率 78.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(CN)CN=C2CCCN2C1
Reaction #1247
amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1=C(COCC=O)NC(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #1346
title compound
収率 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(/C=C/c2ccc3c(c2)C(c2nccs2)=CCC3(C)C)cc1
Reaction #1464
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(N=Nc2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
Reaction #1481
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CF
Reaction #1532
pure title compound
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)NS(=O)(=O)c1sccc1C(=O)CCl
Reaction #1535
pure title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1603
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1605
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1606
5-(4-chlorophenyl)-2-pyrimidinone
収率 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)cnc1=O
Reaction #1607
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1670
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1c(=O)ccc2c(Cl)cccc21
Reaction #1673
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=c1ncc(-c2ccc(Cl)cc2)c[nH]1
Reaction #1674
5-(4-chlorophenyl)-2-pyrimidinone
収率 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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