benzyl piperazine-1-carboxylate

CCCCOc1c(N2CCN(C(=O)OCc3ccccc3)CC2)c(=O)c1=O
Reaction #51226
1-benzyloxycarbonyl-4-(4-butoxy-1,2-dioxo-3-cyclobuten-3-yl)-piperazine
المردود 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)OC(=O)N1CCN(c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cn2)c2ccccc21
Reaction #69984
4-[5-(4-(benzyloxycarbonyl)piperazin-1-yl)pyridin-2-yl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
المردود 74.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(OCc1ccccc1)N1CCN(Cc2ccc(Br)cc2)CC1
Reaction #71628
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(OCc1ccccc1)N1CCN(C(=O)[C@H]2C[C@H](Br)CO2)CC1
Reaction #83067
desired product
المردود 57.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cc2)n1COCC[Si](C)(C)C)C(C)C
Reaction #158966
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-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(N3CCN(C(=O)OCc4ccccc4)CC3)cc2)n1COCC[Si](C)(C)C)C(C)C
Reaction #166920
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-2014_09
CC(C)(C)OC(=O)Nc1ccc(CN2CCN(C(=O)OCc3ccccc3)CC2)cn1
Reaction #172338
benzyl 4-((6-(tert-butoxycarbonylamino)pyridin-3-yl)methyl)piperazine-1-carboxylate
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1CCN(c2cc(N3CCN(C(=O)OCc4ccccc4)CC3)ccc2[N+](=O)[O-])CC1
Reaction #199130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(OCc1ccccc1)N1CCN(c2cccnc2OCc2ccccc2)CC1
Reaction #205022
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)CCC(NC(=O)c1cc(OCC(=O)C(C)(C)C)n(-c2ccccc2)n1)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #206593
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N(N)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #222510
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(CC(=O)N1CCN(C(=O)OCc2ccccc2)CC1)OCC
Reaction #224466
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OCc1ccccc1)N1CCN(c2nc3ccc([N+](=O)[O-])cc3s2)CC1
Reaction #235180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)[Si](C)(C)OCCN1CCN(C(=O)OCc2ccccc2)CC1
Reaction #238556
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #246814
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccccc1CN1CC(=O)N(CCCN2CCN(C(=O)OCc3ccccc3)CC2)C(=O)C1
Reaction #275434
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)CC(O)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #282281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(N)C(=O)N1CCN(C(=O)OCc2ccccc2)CC1.Cl
Reaction #318111
title compound
المردود 67.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(OCc1ccccc1)N1CCN([C@H]2CC[C@H](c3ccc4c(c3)OCO4)CC2)CC1
Reaction #321809
product
المردود 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
O=C(NCc1nccnc1Cl)C1CCC(N2CCN(C(=O)OCc3ccccc3)CC2)CC1
Reaction #332840
title compound
المردود 134.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
الصفحة 1التالي