N-methoxy-N-methylpropanamide

CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #3457
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(=O)Cc1cc(OC)ccc1NC(=O)OC(C)(C)C
Reaction #3477
1-(2-(tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone
Ausbeute 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(=O)c1ccc(OC)cc1C(=O)O
Reaction #58237
5-methoxy-2-propionylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #77730
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCC(=O)Cc1cc(OC)ccc1NC(=O)OC(C)(C)C
Reaction #200454
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)c1ccc(O)c(F)c1
Reaction #234228
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC(=O)c1cc(C)nn2c(-c3sc(-c4cccc(C)n4)cc3C)c(C)nc12
Reaction #284300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC(=O)c1sc2c(-c3cccnc3)ncn2c1CO[Si](CC)(CC)CC
Reaction #317218
2-propionyl-7-(pyridin-3-yl)triethylsilyloxymethylimidazo[5,1-b]thiazole
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCC(=O)c1cscc1Br
Reaction #322284
tan solid
Ausbeute 38.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CCC(=O)c1ccc(C(F)(F)F)cc1C
Reaction #328631
title compound
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #410881
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #456912
1- [2- (tert-butoxycarbonylamino) -6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #483759
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #485037
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #582790
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CCC(=O)c1ccc(I)s1
Reaction #619427
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCC(=O)Cc1c(NC(=O)OC(C)(C)C)cccc1OC
Reaction #653846
1-[2-(tert-butoxycarbonylamino)-6-methoxyphenyl]-2-butanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CCC(=O)Cc1cc(OC)ccc1NC(=O)OC(C)(C)C
Reaction #653865
1-(2-(tert-butoxycarbonylamino)-5-methoxyphenyl]-2-butanone
Ausbeute 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CCc1cc2cc(OC)ccc2[nH]1
Reaction #657809
oil
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1ccc2[nH]c(C(C)C)cc2c1
Reaction #657811
solid
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
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