thiomorpholine

Brc1ccc2c(c1)N=C(N1CCSCC1)c1cccc3c1N2CC3
Reaction #4114
product
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Brc1ccc2c(c1)N=C(N1CCSCC1)c1cccc3c1N2CC3
Reaction #4172
product
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=C1Nc2ccccc2C1=CNc1ccc(OCCCN2CCSCC2)cc1
Reaction #11599
3-{[4-(3-Thiomorpholin-4-yl-propoxy)-phenylamino]-methylene}-1,3-dihydro-indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1Nc2ccccc2C1=CNc1ccc(OCCCCN2CCSCC2)cc1
Reaction #11600
3-{[4-(4-Thiomorpholin-4-yl-butoxy)-phenylamino]-methylene}-1,3-dihydro-indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cn1ncc(C(=O)NC2C3CC4CC(C3)CC2C4)c1N1CCSCC1
Reaction #41140
Methyl-5-thiomorpholin-4-yl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(CN3CCSCC3)ccc21
Reaction #49332
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(thiomorpholinomethyl)indol-2-yl]isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=[N+]([O-])c1ccc(N2CCSCC2)nc1
Reaction #50920
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cc(CN2CCSCC2)cc(OC)c1
Reaction #52984
3,5-dimethoxy-1-(thiomorpholino-methyl)benzene
Yield 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CS(=O)(=O)C(=C1CN([C@@H](c2ccc(Cl)cc2)c2ccc(CN3CCSCC3)cc2)C1)c1cc(F)cc(F)c1
Reaction #53476
1-{(R*)-(4-chlorophenyl)[4-(thiomorpholin-4-ylmethyl)phenyl]methyl}-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
Yield 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(N2CCSCC2)cc1
Reaction #57812
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(C(=O)NC2CC2)cc1-c1ccc(-c2nnc(CN3CCSCC3)o2)cc1
Reaction #59759
N-Cyclopropyl-6-methyl-4′-[5-(thiomorpholin-4-ylmethyl)-1,3,4-oxadiazol-2-yl]-1,1′-biphenyl-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CS(=O)(=O)c1ccc(N2CCSCC2)c(C(=O)N2CCN(c3ccc(C(F)(F)F)cc3)CC2)c1
Reaction #61029
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(Nc1ncnc2cc(C(=O)N3CCSCC3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62504
6-chloro-4-[1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-(thiomorpholin-4-yl-carbonyl)-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc2c(c1)N=C(N1CCSCC1)c1cccc3c1N2CC3
Reaction #62644
product
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Brc1ccc2c(c1)N=C(N1CCSCC1)c1cccc3c1N2CC3
Reaction #63400
product
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1ccc(C(=O)Nc2c(NC(=O)CN3CCSCC3)ccc3c2C(=O)c2ccccc2C3=O)cc1
Reaction #69056
1-(4-methylbenzamido)-2-[2-(1,4-thiazinan-4-yl)acetylamino]-anthraquinone
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1ccc(N2CCSCC2)c(F)c1
Reaction #84372
title compound
Yield 72.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)N=C(NC(=O)OC(C)(C)C)N1CCSCC1
Reaction #159986
(tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(NC(=O)OC(C)(C)C)C(=O)N1CCSCC1
Reaction #164940
(1-Methyl-2-oxo-2-thiomorpholin-4-yl-ethyl)-carbamic acid tert-butyl ester
Yield 98.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCSCC2)cn1
Reaction #170343
title compound
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Page 1Next