#5944673

O=C(Cl)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #332883
benzyl 4-(chlorocarbonyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC1(c2ccc(F)cc2)CCC(C2CNCCN2C(=O)OCc2ccccc2)CC1
Reaction #360921
phenylmethyl [4-(4-fluorophenyl)-4-methoxy-1-cyclohexyl]-1-piperazinecarboxylate
المردود 35.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
N#Cc1ccc(CN2CCN(C(=O)OCc3ccccc3)CC2Cc2cnc[nH]2)cc1
Reaction #364948
1-(4′-Cyanobenzyl)imidazol-5-ylmethyl Piperazine-4-carboxylic Acid Benzyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=C(OCc1ccccc1)N1CCN(Cc2ccc(Br)cc2)CC1
Reaction #375241
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(OCc1ccccc1)N1CCN(c2cc(=O)[nH]cn2)CC1
Reaction #382943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(OCc1ccccc1)N1CCN(c2nc3ccccc3o2)CC1
Reaction #393990
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)OC(=O)N(N)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #404425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1CCN(c2nc(N3CCN(C(=O)OCc4ccccc4)CC3)ccc2[N+](=O)[O-])CC1
Reaction #408531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN(C)CCCN1CCN(C(=O)OCc2ccccc2)CC1
Reaction #429684
brown viscous oil
المردود 103.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cc2)n1COCC[Si](C)(C)C)C(C)C
Reaction #504673
4-{-4-[2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-phenyl}-piperazine-1-carboxylic acid benzyl ester
المردود 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CC(C)(C)OC(=O)N1CCC(N2CCN(C(=O)OCc3ccccc3)CC2)CC1
Reaction #506609
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(OCc1ccccc1)N1CCN(CC2CO2)CC1
Reaction #508025
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C(OCc1ccccc1)N1CCN(CC(O)C(F)(F)F)CC1
Reaction #554699
expected compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(OCc1ccccc1)N1CCN([C@@H]2CCC[C@H]2O)CC1
Reaction #554701
expected compound
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCC1(c2ccccc2)C(=O)NC(=O)N(CCCCC(=O)N2CCN(C(=O)OCc3ccccc3)CC2)C1=O
Reaction #575030
1-[4-(4-Benzyloxycarbonyl-1-piperazinylcarbonyl)butyl]-5-ethyl-5-phenyl-2,4,6(1H,3H,5H)pyrimidinetrione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
CC(C)(C)OC(=O)N(N)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #576115
4-(N-tert-butoxycarbonyl-hydrazinocarbonyl)-piperazine-1-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
C=CS(=O)(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #603576
benzyl 4-(vinylsulfonyl)-1-piperazinecarboxylate
المردود 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
COC(=O)CN1CCN(C(=O)OCc2ccccc2)CC1
Reaction #605896
benzyl 4-(2-methoxy-2-oxoethyl)piperazine-1-carboxylate
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCS(=O)(=O)CCN1CCN(C(=O)OCc2ccccc2)CC1
Reaction #630019
desired product
المردود 812.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
O=C(OCc1ccccc1)N1CCN(C(=O)c2ccccc2)CC1
Reaction #641000
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
السابقالصفحة 2التالي