sodium hydroxide

CCCCCCCCCCOc1cnc(-c2ccc(C(C)O)cc2)nc1
Reaction #1257
(-)-(4-(1-hydroxyethyl) phenyl)-5-decyloxypyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)[C@H](CCCCN)NC(=O)OCc1ccccc1
Reaction #1270
Nα-CBZ-O-t-butyl L-lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N[C@@H]1c2ccccc2C[C@@H]1O
Reaction #1275
cis-1-amino-2-indanol
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CN(CC1CO1)CC1CO1
Reaction #1362
N,N-bis(2,3-epoxypropyl)glycine
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSCc1c(N)c(F)cc(F)c1F
Reaction #1366
2-methylthiomethyl-3,4,6-trifluoroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(Br)cc(Br)c1C(=O)O
Reaction #1382
2-methyl-3-fluoro-4,6-dibromobenzoic acid
Yield 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(Cl)cc2c1c(=O)c(C(=O)O)cn2C1CC1
Reaction #1384
1-cyclopropyl-6-fluoro-7-chloro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(N2CCNCC2)cc2c1c(=O)c(C(=O)O)cn2C1CC1
Reaction #1388
7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Yield 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)N1CCN(c2cc3c(c(C)c2F)c(=O)c(C(=O)O)cn3C2CC2)CC1
Reaction #1390
7-(4-acetyl-1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C2(O)CCCCC2CN(C)C)c1
Reaction #1392
(1RS,2RS)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc([C@]2(O)CCCC[C@H]2CN(C)C)c1
Reaction #1393
(1S,2S)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol
Yield 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[C@@H]1COC(=O)N1
Reaction #1395
(R)-4-tert-butyl-2-oxazolidinone
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(c2cccs2)c2ccc(C(=O)C=Cc3ccc(C(=O)O)cc3)cc21
Reaction #1485
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2ccccc21
Reaction #1486
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
Reaction #1488
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CC=C(Sc2ccccc2)c2cc(C(=O)O)ccc21
Reaction #1493
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1526
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1527
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2sccc2C(O)CF)n1
Reaction #1534
pure title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
Reaction #1540
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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