2-ethyl butanoic acid

CCC1(CC)SC(NC2CCCCCC2)=NC1=O
Reaction #74354
2-(cycloheptylamino)-5,5-diethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCC(CC)C(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #92990
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)OC)c3ccccc3)CC2)c(F)c1
Reaction #197850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(CC)C(=O)Nc1ccc(CCN2C(=O)C(c3ccccc3)(c3ccccc3)N=C2C)cc1
Reaction #207129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(CC)C(=O)N=c1sc2ccccc2n1CCOC
Reaction #242028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(CC)C(=O)OC
Reaction #278191
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC(CC)C(=O)c1ccc(OC)cc1
Reaction #366880
para-methoxy-2-ethylbutyrophenone
收率 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)C1CCCN1C(=O)C(CC)CC
Reaction #391922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(CC)C(=O)OCCCn1ccc2cc(C[C@@H](C)N(CCOc3ccccc3OCC(F)(F)F)C(=O)OC(C)(C)C)cc(C(N)=O)c21
Reaction #469658
(R)-3-[5-[2-[N-(tert-butoxycarbonyl)-N-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-7-carbamoyl-1H-indol-1-yl]propyl 2-ethylbutyrate
收率 71.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCC(CC)C(=O)Nc1ccc(CCN2C(=O)C(c3ccccc3)(c3ccccc3)N=C2C)cc1
Reaction #594582
2-ethyl-N-{4-[2-(2-methyl-5-oxo-4,4-diphenyl-4,5-dihydro-imidazol-1-yl)-ethyl]-phenyl}-butyramide
收率 35.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCC(CC)C(=O)N1CCC(NC(=O)Nc2ccc(OC(F)(F)F)cc2)CC1
Reaction #661871
desired compound
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCC(CC)C(=O)N1CCC(NC(=O)Nc2ccc(C(F)(F)F)cc2)CC1
Reaction #661872
desired compound
收率 55.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCC(CC)C(=O)N=c1sc(C)c(C)n1CCOC
Reaction #757283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCC(CC)C(=O)OCCCn1ccc2cc(CC(C)N(CCOc3ccccc3OCC(F)(F)F)C(=O)OC(C)(C)C)cc(C(N)=O)c21
Reaction #905255
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC1(CC)SC(NC2CCCCCC2)=NC1=O
Reaction #939910
2-(cycloheptylamino)-5,5-diethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CCC1(CC)SC(NC2CCCCCC2)=NC1=O
Reaction #1245219
2-(cycloheptylamino)-5,5-diethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCC(CC)C(=O)OCC(=O)OC1C(CC)CC2C3CCC4=CC(=O)CCC4C3CCC21C
Reaction #1296631
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCC(CC)C(=O)OC
Reaction #1856231
methyl 2-ethylbutyrate
收率 53.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
CCOC(=O)[C@@H]1CCCN1C(=O)C(CC)CC
Reaction #1880968
desired product
收率 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_04
CCC(CC)NC(=O)Nc1ccc(Cl)c(S(N)(=O)=O)c1O
Reaction #1972083
6-Chloro-3-[3-(1-ethyl-propyl)-ureido]-2-hydroxy-benzenesulfonamide
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_07
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