methanol

COc1ccc2ccc(N)nc2n1
Reaction #1004
2-methoxy-7-amino-1,8-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(N)COc1ccc(C#N)cc1
Reaction #1019
desired product
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(Cl)ccc1OCC(C)N
Reaction #1020
desired product
Yield 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(N)C(C)Oc1ccc(Cl)cc1
Reaction #1021
desired product
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1nccc2ccccc12
Reaction #1026
1-acetyl-isoquinoline oxime
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=NO)c1cc2ccccc2cn1
Reaction #1028
3-acetyl-isoquinoline oxime
Yield 89.0%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
Yield 45.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(Oc2ccc(C3CCNCC3)cc2)cc1
Reaction #1047
compound ( 4 )
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)O
Reaction #1091
2-methoxycarbonyl-5-nitrobenzenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc([N+](=O)[O-])cc1S(=O)(=O)Cl
Reaction #1092
2-Methoxycarbonyl-5-nitrobenzenesulfonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(N)cc1S(=O)(=O)NC(C)(C)C
Reaction #1093
N-tert-Butyl-5-amino-2-methoxycarbonylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(NC2CCC3(CC2)OCC(C)(C)CO3)ccnc1C
Reaction #1100
4-(3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-ylamino)-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
CN1CCCC1c1cncc(-c2ccc(Cl)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1127
5-(4-chlorophenyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(-c2ccc(F)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1128
5-(4-fluorophenyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(-c2ccco2)c1.O=C(O)/C=C/C(=O)O
Reaction #1129
5-(2-furanyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc([Si](C)(C)C)c1.O=C(O)/C=C/C(=O)O
Reaction #1130
5-trimethylsilyl-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(C#Cc2ccccc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1131
5-(phenylethynyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#Cc1cncc(C2CCCN2C)c1
Reaction #1132
5-ethynyl-3-(1-methyl-2-pyrrolidinyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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