D-valinol

COC(=O)N[C@@H](CO)C(C)C
Reaction #5035
N-Methyloxycarbonyl-D-valinol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(S(=O)(=O)n2cc(-c3nc(N[C@@H](CO)C(C)C)ncc3C#N)c3cc(C)cnc32)cc1
Reaction #69150
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)[C@H](CO)Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1S(=O)CC2
Reaction #157283
(R)-2-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-ylamino}-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)[C@H](CO)Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1[S@](=O)CC2
Reaction #330823
(R)-2-{(R)-2-[4-(4-Chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-ylamino}-3-methyl-butan-1-ol
Ausbeute 178.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)[C@@H]1COCC(=O)N1
Reaction #337114
(R)-5-isopropylmorpholin-3-one
Ausbeute 69.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CCOC(=O)C(CCc1ccccc1)N[C@H]1CSC[C@@H](C(C)C)N(CC(=O)OC(C)(C)C)C1=O
Reaction #343216
t-Butyl α-[6(R)-(1-ethoxycarbonyl-3-phenylpropylamino)-3(R)-isopropyl-5-oxoperhydro-1,4-thiazepin-4-yl]acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
CC(C)[C@H](CO)Nc1nc(Cl)ncc1I
Reaction #359814
(R)-2-(2-Chloro-5-iodo-pyrimidin-4-ylamino)-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCc1cnc(Cl)nc1N[C@@H](CO)C(C)C
Reaction #359821
product
Ausbeute 60.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1cc([N+](=O)[O-])ccc1N=C1N[C@H](C(C)C)CS1
Reaction #363672
(4R)-2-(2-methyl-4-nitrophenylimino)-4-isopropyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #418055
(R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)Nc1cccnc1N1CCN(C(=O)c2ccc(C(=O)N[C@@H](CO)C(C)C)cn2)CC1
Reaction #468538
desired compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #493086
(R)-2-(2-chloro-6,7-dihydrothieno[3,2-d]pyrimidin-4-ylamino)-3-methylbutan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #495267
(R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #537033
(R)-2-(2-chloro-6,7-dihydrothieno[3,2-d]pyrimidin-4-ylamino)-3-methylbutan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #561339
(R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
COC[C@H](Nc1c(Nc2ccc(Cl)c(S(=O)(=O)N(C)OC)c2O)c(=O)c1=O)C(C)C
Reaction #604088
6-Chloro-2-hydroxy-N-methoxy-3-[2-((R)-1-methoxymethyl-2-methyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-N-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)[C@H](CO)Nc1nc(Cl)nc2c1SCC2
Reaction #605196
(R)-2-(2-chloro-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ylamino)-3-methyl-butan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CNC(=O)c1c(-c2ccc(F)cc2)oc2ccc(-c3cccc(C4=N[C@H](C(C)C)CO4)c3)cc12
Reaction #642234
titled compound
Ausbeute 26.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4cccc(CN[C@@H](CO)C(C)C)c4)cc23)CC1
Reaction #649231
title compound
Ausbeute 32.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1ccc(S(=O)(=O)n2cc(-c3nc(N[C@@H](CO)C(C)C)ncc3C#N)c3cc(C)cnc32)cc1
Reaction #974554
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
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