1,3-diamino-2-propanol

NCC(O)CNC(=O)CCCCCCCCCCCO
Reaction #1220
title compound
Ausbeute 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C1=NCC(O)CN1
Reaction #270894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)C2CCC(C2)C1CCC(CCC1C2CCC(C2)C1(C)C)NCC(O)CN
Reaction #285722
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1ccccc1Oc1ccccc1[C@](O)(CCCCOC)[C@@H]1CCCN(C(=O)NCC(O)CN)C1
Reaction #340776
(3R)-3-((S)-1-(2-(2-ethylphenoxy)phenyl)-1-hydroxy-5-methoxypentyl)-N-(3-amino-2-hydroxypropyl)piperidine-1-carboxamide
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)C(N)C(=O)CNS(=O)(=O)c1ccc(Oc2cccc(Cl)c2C#N)cc1
Reaction #499269
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
NCC(O)CNC(CCc1ccccc1)CCc1ccccc1
Reaction #514091
1-amino-3-[1,5-di-(phenyl)-3-pentylamino]-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_10
NCC(O)CNC(CCc1ccccc1)CCc1ccccc1
Reaction #530710
1-amino-3-[1,5-di-(phenyl)-3-pentylamino]-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
CC1(C)C2CCC(C2)C1CCC(CCC1C2CCC(C2)C1(C)C)NCC(O)CN
Reaction #549509
1-amino-3-[1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylamino]-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_12
OC1CN=C(C(F)(F)F)NC1
Reaction #561836
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1ccc2nc(N3CCS(=O)(=O)c4ccccc4C3)cc(NCC(O)CN)c2c1
Reaction #627260
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
NC1=NCC(CNc2cc(N3CCCc4ccccc4C3)nc3ccc(Cl)cc23)O1
Reaction #627510
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
OC(CNCc1ccccn1)CN(Cc1ccccn1)Cc1ccccn1
Reaction #687304
aimed product
Ausbeute 25746.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)C(N)C(=O)CNS(=O)(=O)c1ccc(Oc2cccc(Cl)c2C#N)cc1
Reaction #697590
title compound
Ausbeute 2.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CC1(C)C2CCC(CC2)C1CCC(CCC1C2CCC(CC2)C1(C)C)NCC(O)CN
Reaction #751923
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
N=C1NCC(O)CN1
Reaction #778920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
OC1CN=C(C(F)(F)F)NC1
Reaction #793075
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCc1ccccc1Oc1ccccc1C(O)(CCCCOC)C1CCCN(C(=O)NCC(O)CN)C1
Reaction #905911
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cl
Reaction #918064
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
OC1CN=C(C(F)(F)F)NC1
Reaction #920854
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC1(C)C2CCC(CC2)C1CCC(CCC1C2CCC(CC2)C1(C)C)NCC(O)CN
Reaction #953897
1-amino-3-[1,5-di-(3,3-dimethylbicyclo[2.2.2]oct-2-yl)-3-pentylamino]-2-propanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_07
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