hydrochloric acid

c1ccc(Cn2cnc3c(OC4CN5CCC4CC5)nccc32)cc1
Reaction #1010
title compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(COc1ccc(C#N)cc1)NC(=O)[C@@H](N)C(C)C.Cl
Reaction #1024
desired product
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P(O)(O)CC(F)=C(F)F
Reaction #1046
2,3,3-trifluoro-2-propenylphosphonic acid
Ausbeute 45.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2cc(B(O)O)sc2c1
Reaction #1089
6-methoxybenzo[b]thiophene-2-boronic acid
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(N(CC2=CCC(O)(C(C)(C)C)C=C2)C2CCCCC2)ccnc1C
Reaction #1104
4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(O)(CCC)N(c1ccnc(C)c1OC)C1CCCCC1
Reaction #1105
4-[(4-Hydroxy-4-n-octyl)cyclohexylamino]-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(NC2CCC(C(C)(C)C)CC2)ccnc1C
Reaction #1107
4-(4-tert-Butylcyclohexylamino)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1124
2-Methoxy-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCC#N)oc2c1
Reaction #1147
2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran
Ausbeute 83.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1oc(-c2ccccc2)nc1COc1ccc2cc(CCCCC#N)oc2c1
Reaction #1148
2-(4-cyanobutyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nn2cc[nH]c2c1-c1ccc(N)cc1.Cl
Reaction #1168
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.NNc1ccc(C(=O)O)c2c1CCCC2
Reaction #1178
hydrazine
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #1179
expected product
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(C(=O)O)ccc1NN.Cl
Reaction #1180
4-Hydrazino-3-methoxybenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.N#Cc1ccc(NN)cc1Cl
Reaction #1181
2-Chloro-4-hydrazinobenzonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.NNc1ccc(Cl)c(C(=O)O)c1
Reaction #1182
expected product
Ausbeute 123.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C(=O)O)cc1NN.Cl
Reaction #1183
3-Hydrazino-4-methylbenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCCCOCC(C)(O)CCNCCO
Reaction #1201
title compound
Ausbeute 30.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(=O)C(=NO)C(=O)c1c(C)cc(C)cc1C
Reaction #1249
semi-solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1nn(C)c(-c2c(C)cc(C)cc2C)c1N
Reaction #1250
title compound
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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