#5944669

O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
Reaction #75587
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(OCc1ccccc1)N1CCC(O)(CF)CC1
Reaction #75590
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(OCc1ccccc1)N1CCC(O)(CNc2cccc(F)c2)CC1
Reaction #224933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OCc1ccccc1)N1CCC(O)(CNc2ccc(F)cc2)CC1
Reaction #295384
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
Reaction #886049
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(OCc1ccccc1)N1CCC(O)(CF)CC1
Reaction #893367
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
N#Cc1ccc(NCC2(O)CCN(C(=O)OCc3ccccc3)CC2)cc1
Reaction #1218801
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(OCc1ccccc1)N1CCC(O)(CNC2CCCCC2)CC1
Reaction #1232610
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
NCC1(O)CCNCC1
Reaction #1683853
4-aminomethyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_09
N#Cc1ccc(NCC2(O)CCN(C(=O)OCc3ccccc3)CC2)cc1
Reaction #1683856
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_09
NCC1(O)CCNCC1
Reaction #1947458
4-aminomethyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
O=C(OCc1ccccc1)N1CCC(O)(CNC2CCCCC2)CC1
Reaction #2123274
product
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
O=C(OCc1ccccc1)N1CCC(O)(CNCC2CC2)CC1
Reaction #2123275
benzyl 4-{[(cyclopropylmethyl)amino]methyl}-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
O=C(OCc1ccccc1)N1CCC(O)(CNc2cccc(F)c2)CC1
Reaction #2123278
benzyl 4-{[(3-fluorophenyl)amino]methyl}-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
O=C(OCc1ccccc1)N1CCC(O)(CNc2ccc(F)cc2)CC1
Reaction #2123279
benzyl 4-{[(4-fluorophenyl)amino]methyl}-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
NCC1(O)CCNCC1
Reaction #2208134
4-aminomethyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_02
N#Cc1ccc(NCC2(O)CCN(C(=O)OCc3ccccc3)CC2)cc1
Reaction #2208137
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_02
O=C(OCc1ccccc1)N1CCC(F)(CO)CC1
Reaction #2387327
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_12
O=C(OCc1ccccc1)N1CCC(O)(CF)CC1
Reaction #2387330
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_12
O=C(OCc1ccccc1)N1CCC(O)(CNCC2CC2)CC1
Reaction #2401204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)