rac-2-(hydroxymethyl)piperazine

COC(=O)N1CCNC(CO)C1
Reaction #256107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)N1CCNC(CO)C1
Reaction #279838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCNC(CO)C3)cc21.Cl
Reaction #335643
1-Ethyl-6-fluoro-1,4-dihydro-7[3-(hydroxymethyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
COc1ccc(CS[C@H]2C[C@@H](C(=O)N3CCNC(CO)C3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #449226
title compound
Yield 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
NS(=O)(=O)Cc1cccc(Nc2ncnc(N3CCNCC3CO)n2)c1
Reaction #674330
rac-3-[(4-(2-(Hydroxymethyl)piperazin-1-yl)-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1ccc(CS[C@H]2C[C@@H](C(=O)N3CCNC(CO)C3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #814837
title compound
Yield 56.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
OCC1CN(c2nnc(-c3ccc(F)cc3)c3ccccc23)CCN1
Reaction #1326215
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COc1ccc(CSC2CC(C(=O)N3CCNC(CO)C3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #2222563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCNC(CO)C3)cc21.Cl
Reaction #2252788
1-Ethyl-6-fluoro-1,4-dihydro-7-[3-(hydroxymethyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_07
N
Reaction #2253257
ammonia
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_07