(S)-1-amino-2-propanol

C[C@H](O)CNc1ccccn1
Reaction #992
title compound
Выход 84.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@H](O)CNC(=S)NC(C)(C)C
Reaction #76023
N-[(2S)-2-hydroxypropyl]-N′-tert-butylthiourea
Выход 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N
Reaction #79580
ammonia
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[C@H](O)CNC(=O)C(O)c1ccc(-c2noc(-c3onc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164351
2-hydroxy-N—((S)-2-hydroxypropyl)-2-(4-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Выход 44.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@H](O)CNC(=O)C(O)c1ccc(-c2noc(-c3cnn(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164361
(R/S)-2-hydroxy-N-((S)-2-hydroxypropyl)-2-(4-(5-(1-phenyl-5-(trifluoromethyl)-1H-pyrazol-4-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Выход 44.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@H](O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164367
(R/S)-2-hydroxy-N—((S)-2-hydroxypropyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
Выход 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[C@H](O)CNC(=O)c1ccc2c(c1)OCCc1cc(C(=O)N(C)c3ccccc3Cl)sc1-2
Reaction #171666
177
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CSc1nc(NC[C@@H](C)O)c2cnn(COCC[Si](C)(C)C)c2n1
Reaction #317365
(R)-1-[6-Methylsulfanyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol
Выход 107.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CSc1nc(NC[C@@H](C)O)c2c(C3CCCC3)n[nH]c2n1
Reaction #317380
(R)-1-(3-Cyclopentyl-6-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino)-propan-2-ol
Выход 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
C[C@@H](O)CNc1nc2c(-c3ccccc3Cl)n[nH]c2nc1Oc1ccc(F)cc1F
Reaction #317387
(R)-1-[3-(2-Chloro-phenyl)-6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-b]pyrazin-5-ylamino]-propan-2-ol
Выход 11.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
—
Reaction #326732
solid
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
—
Reaction #326749
foam
Выход 35.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C[C@H](O)Cn1ccc2c1-c1cc(F)ccc1C2
Reaction #351630
(S)-1-(7-fluoro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol
Выход 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COc1ccc2c(c1)-c1c(ccn1C[C@H](C)O)C2
Reaction #351632
(S)-1-(7-methoxy-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
C[C@H](O)Cn1ccc2c1-c1cc(Cl)ccc1C2
Reaction #351634
(S)-1-(7-chloro-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COc1ccc2c(c1)-c1c(ccn1CC(C)O)CC2
Reaction #351636
4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl-propan-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
C[C@H](O)Cn1ccc2c1-c1ccccc1OC2
Reaction #351718
(S)-1-(1,4-dihydro-[1]benzopyrano[4,3-b]pyrrol-1-yl)-propan-2-ol
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
—
Reaction #359833
( R )-
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
Cc1ccc(C(=O)NC2CC2)cc1-n1ccnc(NC2(c3ccccc3OCCNC[C@H](C)O)CC2)c1=O
Reaction #424260
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Cc1ccc(C(=O)NC[C@H](C)O)cc1-n1cnc(OCc2ccc(F)cc2F)c(Br)c1=O
Reaction #438132
desired product
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
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