2-amino-1-propanol

CC(N)COc1ccc(C#N)cc1
Reaction #1022
desired product
수율 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(N)COc1ccncc1
Reaction #1023
desired product
수율 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(CO)NCc1ccc2c(c1)cc(-c1ccc(Cl)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49314
4-chloro-7-{1-(tert-butoxycarbonyl)-5-[(2-hydroxy-1-methylethyl)aminomethyl]indol-2-yl}isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(CO)NC(=N)c1c(O)nsc1Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62042
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(CO)NC(=N)c1c(O)nsc1Nc1ccc(C(=O)C2CNc3ccccc32)cc1
Reaction #62045
5-[4-(2,3-dihydro-indole-1-carbonyl)-phenylamino]-3-hydroxy-N-(2-hydroxy-1-methyl-ethyl)-isothiazole-4-carboxamidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCCCCCCCCCCCCC(=O)NC(C)CO
Reaction #62582
title compound
수율 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NC(C)CO
Reaction #72236
title compound
수율 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)NC(C)CO)cn1
Reaction #170501
title compound
수율 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(CO)NC(=O)c1ccc(OCc2conc2-c2ccc(F)cc2)nc1
Reaction #170609
title compound
수율 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@H](CO)NC(=O)c1ccc(OCc2conc2-c2ccc(F)cc2)nc1
Reaction #170610
title compound
수율 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(CO)NC(=O)c1ccc(N(C)C(=O)c2cc3c(s2)-c2ccccc2OCC3)c(Cl)c1
Reaction #171710
228
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccn2)c1COc1cc(C(=O)NC(C)CO)nn1C
Reaction #176727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-c2cc(C(=O)NC(C)CO)cc(-n3nnnc3C(C)(F)F)c2)nc1
Reaction #177320
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)Nc1nc(SCc2ccccc2)nc2nc(N)sc12
Reaction #180380
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)N1CCN(c2cccc3c2OCCO3)CC1
Reaction #180506
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)Nc1ccc(C#N)cc1Cl
Reaction #182365
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)Nc1cc(N)nc(SCc2ccccc2F)n1
Reaction #183664
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)NC(C)CO
Reaction #185810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)Nc1nc(SCc2cccc(F)c2F)nc2[nH]c(=O)cnc12
Reaction #191202
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(CO)NCc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #192019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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