(1S)-1-(hydroxymethyl)-3-methylbutylamine

CC(C)C[C@@H](CO)NCCCS(=O)(=O)O
Reaction #326950
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)C[C@@H](CO)NC(=O)c1cn(COCC[Si](C)(C)C)c2ncc(-c3nn(C)c4cc(F)ccc34)nc12
Reaction #333363
2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-1-hydroxymethyl-3-methyl-butyl)-amide
Ausbeute 59.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)C[C@H]1COCC(=O)N1
Reaction #337041
(S)-5-iso-butylmorpholin-3-one
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)C[C@H]1COC(C(C)C)N1
Reaction #363441
(4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)CC1CN(CC(C)C)C(=Nc2cnc3ccccc3c2)S1
Reaction #363613
2-(3-quinolylimino)-3,5-diisobutyl-1,3thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)CC1CN(CC(C)C)C(=Nc2ccc([N+](=O)[O-])cc2)S1
Reaction #363614
2-(4-nitrophenylimino)-3,5-diisobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)CC1CN(CC(C)C)C(=Nc2ccc(C#N)cc2)S1
Reaction #363615
2-(4-cyanophenylimino)-3,5-diisobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363616
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@H](CC(C)C)CS1
Reaction #363617
(4R)-2-(2-methyl -4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc([N+](=O)[O-])cc1N=C1N[C@H](CC(C)C)CS1
Reaction #363618
(4R)-2-(2-methyl-5-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc([N+](=O)[O-])cc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363619
(4S)-2-(2-methyl-5-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@H](CC(C)C)CS1
Reaction #363620
(4R)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363621
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1ccc([N+](=O)[O-])cc1N=C1N[C@H](CC(C)C)CS1
Reaction #363622
(4R)-2-(2-methyl-5-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363623
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363624
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363626
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363628
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363630
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@@H](CC(C)C)CS1
Reaction #363631
(4S)-2-(2-methyl-4-nitrophenylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
Seite 1Weiter