tryptamine

O=C(NCCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)NCCc1c[nH]c2ccccc12)OCc1ccccc1
Reaction #11955
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCCc3c[nH]c4ccccc34)n2)c1
Reaction #42995
N-(3-Amino-propyl)-N-(3-{2-[2-(1H-indol-3-yl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1NC(=O)c2ccccc21
Reaction #55514
phthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
NCCCC[C@H](N)C(=O)O
Reaction #72415
lysine
수율 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(Cc1c[nH]c2ccccc12)(NC(=O)OC1C2CC3CC(C2)CC1C3)C(=O)NCCc1c[nH]c2ccccc12
Reaction #83127
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCN[C@@H]1C[C@H]2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92664
5α-Hydroxy-6β-(3-propylamino)-cholestan-3β-ol
수율 71.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCN[C@@H]1C=C2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92669
5α-Hydroxy-6β-(3-propylamino)-cholest-7-en-3β-ol
수율 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Oc1cccc(Nc2nc(NCCc3c[nH]c4ccccc34)ncc2F)c1
Reaction #158649
5-fluoro-N4-(3-hydroxyphenyl)-N2-[2-(indol-3-yl)ethyl]-2,4-pyrimidinediamine
수율 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Oc1cccc(Nc2nc(NCCc3c[nH]c4ccccc34)ncc2F)c1
Reaction #163758
5-fluoro-N4-(3-hydroxyphenyl)-N2-[2-(indol-3-yl)ethyl]-2,4-pyrimidinediamine
수율 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN(C)C1(c2cccc(F)c2)CCC(=CC(=O)NCCc2c[nH]c3ccccc23)CC1
Reaction #177686
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CCc1cnoc1-c1ccccc1)NCCc1c[nH]c2ccccc12
Reaction #180221
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2NCCc3c2[nH]c2ccccc32)cc1
Reaction #180333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(C2NCCc3c2[nH]c2ccccc32)cc1
Reaction #186059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2c3c([nH]c2c1)C(c1ccc2c(c1)CCC2)NCC3
Reaction #187222
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NCCc1c[nH]c2ccccc12)c1cccnc1
Reaction #204173
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1ccc(C2NCCc3c2[nH]c2ccccc32)cc1
Reaction #210285
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1CCc1c[nH]c2ccccc12
Reaction #210995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)NCC(=O)NCCc1c[nH]c2ccccc12
Reaction #211994
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1CCc1c[nH]c2ccccc12
Reaction #213680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(S(=O)(=O)NCCc2c[nH]c3ccccc23)cc1
Reaction #225472
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
1 페이지다음 페이지