methyl 3-bromomethyl-2-thiophenecarboxylate

COC(=O)c1sccc1COc1cccc(NC(C)=O)c1
Reaction #1925
methyl 3-(3-acetamidophenoxymethyl)-2-thiophenecarboxylate
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1sccc1C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
Reaction #1927
2-methoxycarbonylthiophen-3-ylmethyltriphenylphosphonium bromide
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1sccc1CBr
Reaction #197406
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Br-]
Reaction #236012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1sccc1CSc1cccc(N)c1
Reaction #294545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1sccc1CBr
Reaction #304446
Intermediate
Ausbeute 68.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)c1sccc1COC(C)=O
Reaction #378314
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)CSc1ccc(OCc2ccsc2C(=O)OC)cc1
Reaction #408748
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1sccc1CSc1cccc(N)c1
Reaction #409410
methyl 3-(3-aminophenylthiomethyl)thiophene-2-carboxylate
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)CSc1ccc(OCc2ccsc2C(=O)OC)cc1
Reaction #476209
captioned compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COC(=O)c1sccc1COc1ccc(C(C)CCCO)cc1
Reaction #725437
product
Ausbeute 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_12
COC(=O)c1sccc1COc1ccc(C(C)CCCO)cc1
Reaction #1021914
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1sccc1CN
Reaction #1290665
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
COC(=O)c1sccc1CBr
Reaction #1453373
title compound
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COC(=O)c1sccc1CN
Reaction #1453374
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COC(=O)c1sccc1CBr
Reaction #1649882
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
COC(=O)c1sccc1COC(C)=O
Reaction #1854127
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
COC(=O)c1sccc1CBr
Reaction #1859303
116c
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
COC(=O)c1sccc1CN
Reaction #1859304
116d
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_02
COC(=O)c1sccc1CBr
Reaction #2008999
title compound
Ausbeute 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
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