thiopene-2-carbonyl chloride

O=C(NCCCSc1ccncc1)c1cccs1
Reaction #6212
desired compound
수율 70.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCCCSc1ccccn1)c1cccs1
Reaction #6213
desired compound
수율 85.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCCCSc1cccnc1)c1cccs1
Reaction #6214
desired compound
수율 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(NCCCOc1ccncc1)c1cccs1
Reaction #6239
desired compound
수율 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)(C)OC(=O)N1CCN(C(=O)c2cccs2)CC1
Reaction #6785
solids
수율 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(CNC(=O)c4cccs4)c3C2=O)C(=O)N1
Reaction #10069
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-2-thienylcarboxamide
수율 47.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1csc(-c2nn3c(Cc4ccc5c(c4)OCO5)nnc3s2)c1
Reaction #40720
compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCN(C(=O)c2cccs2)CC1
Reaction #42634
solids
수율 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3cccs3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43882
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(c1cccs1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50674
2-[2-(2-Thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H) dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COc1ccc(C(=O)c2cccs2)c(C(=O)O)c1
Reaction #58208
5-Methoxy-2-(thiophene-2-carbonyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cccc(NC(=O)c2cccs2)c1
Reaction #66516
N-(3-methoxyphenyl)thiophene-2-carboxamide
수율 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cl.O.O=C(NC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1)c1cccs1
Reaction #78352
expected product
수율 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(Nc1ccc(C#CCCN2CC=C(c3ccccc3)CC2)nc1)c1cccs1
Reaction #81925
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(Nc1nc2c(s1)Cc1ccccc1-2)c1cccs1
Reaction #176141
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C2(O)CCCN(C(=O)c3cccs3)C2)c1
Reaction #183276
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)N(NC(=O)c1ccccc1)C(=O)c1cccs1
Reaction #184892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(F)c([N+](=O)[O-])c1)c1cccs1
Reaction #194308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1nc(-c2cccc(C)c2)c(-c2ccnc(NC(=O)c3cccs3)c2)s1
Reaction #209576
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2ccc(F)c([N+](=O)[O-])c2)c1
Reaction #209704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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