#1041126

N[C@@H](Cc1ccc(O)cc1)C(=O)O
Reaction #5843
Tyrosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)OCOC(=O)C(C)(C)C)=C(C3CCC(=O)O3)CS[C@H]12)c1csc(N)n1
Reaction #6391
title compound
収率 59.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1COC2(CCN(C(=O)OCc3ccccc3)CC2)C(Cc2ccc(F)cc2)N1
Reaction #40649
title compound
収率 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2nc(NC(=O)C(CC3CCC(F)(F)CC3)c3ccc4c(c3)Nc3ccccc3S4(=O)=O)sc2n1
Reaction #43276
3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Nc1ccn(Cc2ccccc2)n1)C(CC1CCC(F)(F)CC1)c1ccc2c(c1)Nc1ccccc1S2(=O)=O
Reaction #43277
N-(1-benzyl-1H-pyrazol-3-yl)-3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1ccc(NC(=O)C(CC2CCC(F)(F)CC2)c2ccc3c(c2)Nc2ccccc2S3(=O)=O)n1
Reaction #43278
3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOP(=O)(OCC)C1CC[C@H]2COC[C@@H](c3cc(F)c(F)c(F)c3)N2C1=O
Reaction #44629
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC[PH](=O)C(CCC/C=C(/C)CCC=C(C)C)P(=O)(OCC)OCC
Reaction #50484
pale yellow oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(C#CCCCO)cc1
Reaction #53378
product 16
収率 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCNC1(Cl)C=CN(c2cccnc2)N1
Reaction #85364
3-chloro-N-ethyl-1-(pyridin-3-yl)-1H-pyrazol-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)[C@H](CI)NC(=O)OC(C)(C)C
Reaction #87114
(R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate
収率 68.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)[C@H](CI)NC(=O)OCc1ccccc1
Reaction #87130
(R)-methyl 2-(benzyloxycarbonylamino)-3-iodopropanoate
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(CCC(C#N)(c1ccc(OC)c(OC)c1)C(C)C)OCC
Reaction #93575
formula 6
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(c1cc2cnn(C)c2cc1F)c1cnc2ccc(-c3cnn(C)c3)nn12
Reaction #156461
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cn1ncc2cc(Cc3cnc4ccc(Cl)nn34)c(F)cc21
Reaction #156467
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCN(CC)C(=O)CCC(=O)OCI
Reaction #173038
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CNc1cccc(OCc2ccccc2)c1NC(C)=O
Reaction #173142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc2c(c1)cnn2-c1ccc(OCCCN2CCCC2)cc1
Reaction #173206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)C3CSCCN43)CC2)nc1
Reaction #173448
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(OCCCN(CCC(N)=O)Cc2ccccc2)ccc1Cc1c(OC2OC(COC(=O)C(C)(C)C)C(OC(=O)C(C)(C)C)C(OC(=O)C(C)(C)C)C2OC(=O)C(C)(C)C)n[nH]c1C(C)C
Reaction #173585
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
1 ページ次のページ