ethyl 2-bromoisobutyrate

CCOC(=O)C(C)(C)Oc1ccc(C(C)=O)cc1C
Reaction #9722
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1ccc(C(C)=O)cc1C
Reaction #9796
Intermediate 5
Ausbeute 159.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)(C)OCCc1ccc(Br)cc1
Reaction #59829
title compound
Ausbeute 15.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C(C)(C)Oc1cccc(C2(O)CCN(C(=O)c3ccc(Br)cc3)CC2)c1
Reaction #64141
ethyl 3-{1-(4-bromobenzoyl)-4-hydroxypiperidin-4-yl}α,α-dimethylphenoxyacetate
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C(C)(C)NNC(=O)OCc1ccccc1
Reaction #67932
2-(N′-benzyloxycarbonyl-hydrazino)-2-methyl-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)NCCNC1=O
Reaction #71414
3,3-dimethyl-piperazin-2-one
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)NCCNC1=O
Reaction #71418
title compound
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)(C)Sc1cccnc1-c1ccc(C#N)cc1
Reaction #74047
ethyl 2-(2-(4-cyanophenyl)pyridin-3-ylthio)-2-methylpropanoate
Ausbeute 49.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)(C)Sc1ccncc1Br
Reaction #74049
ethyl 2-(3-bromopyridin-4-ylthio)-2-methylpropanoate
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)(C)Sc1ncccc1Br
Reaction #74055
ethyl 2-(3-bromopyridin-2-ylthio)-2-methylpropanoate
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)SC(NC2CC3CCC2C3)=NC1=O
Reaction #74318
2-(bicyclo[2.2.1]hept-2-ylamino)-5,5-dimethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)SC(NCC2CCCCC2)=NC1=O
Reaction #74327
2-[(cyclohexylmethyl)amino]-5,5-dimethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)SC(NC2CCCCCCC2)=NC1=O
Reaction #74346
2-(Cyclooctylamino)-5,5-dimethyl-1,3-thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C(C)(C)Oc1cccc(F)c1
Reaction #84552
title compound
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C(C)(C)Oc1ccc2c(c1)c(-c1ccccc1)c(C)n2C
Reaction #95109
2-Methyl-2-[1,2-dimethy-3-phenyl-1H-indole-5-yloxy]propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C(C)(C)Oc1ccc2c(c1)c(-c1ccc(OC)cc1)c(C)n2C
Reaction #95110
2-[3-(4-Methoxy-phenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccc(OC)cc3)c2c1
Reaction #95111
2-[3-(4-Methoxy-phenyl)-2-methyl-1H-indole-5-yloxy]-2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCn1c(C)c(-c2ccc(OC)cc2)c2cc(OC(C)(C)C(=O)OCC)ccc21
Reaction #95112
2-[3-(4-Methoxy-phenyl)-2-methyl-1-propyl-1H-indole-5-yloxy]-2-methylpropanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)C(C)(C)Oc1ccc2[nH]c(C)c(-c3ccccc3Cl)c2c1
Reaction #95113
2-[3-(2-Chloro-phenyl)-2-methyl-1H-indole-5-yloxy]2-methyl-propanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCCn1c(C)c(-c2ccccc2Cl)c2cc(OC(C)(C)C(=O)OCC)ccc21
Reaction #95114
2-[3-(2-Chloro-phenyl)-2-methyl-1-propyl-1H-indole-5-yloxy]-2-methylpropanoic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
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