1,3-thiazolidine

CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1)C(=O)O
Reaction #6712
H-Pro-Ile
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1c(OC(F)F)cccc1S(=O)(=O)N1CCSC1
Reaction #67501
2-difluoromethoxy-6-(thiazolidine-3-sulfonyl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1c(F)cccc1S(=O)(=O)N1CCSC1
Reaction #67502
2-fluoro-6-(thiazolidine-3-sulfonyl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(C5SCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #159067
(1-{2-[5-(4′-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-yl]-thiazolidine-3-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(NC1(C(=O)O)CCCCC1)N1CCSC1
Reaction #161014
title compound
Rendement 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(C5SCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #167016
(1-{2-[5-(4′-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-yl]-thiazolidine-3-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCSC2)cn1
Reaction #170537
title compound
Rendement 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC(C)C(=O)N1CCSC1
Reaction #181905
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N2CCSC2)cn1
Reaction #191050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1c(OC(F)F)cccc1S(=O)(=O)N1CCSC1
Reaction #192782
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1nc(N2CCOCC2)nc(N2CCSC2)n1
Reaction #202437
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C=CC(=O)NC2CCC(C)CC2)ccc1OCCNCCS
Reaction #235846
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1ccccc1)C(CN1CCSC1)c1ccccc1
Reaction #240454
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC[NH+](CC)CC
Reaction #247637
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CC(O)CCc1ccc(-c2ccccc2)cc1)N1CCSC1
Reaction #251631
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)N1CCSC1
Reaction #253966
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(Cn1c(-c2ccc(Cl)cc2)nc2cccnc21)N1CCSC1
Reaction #269462
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NC(CCOc1ccccc1)c1ccccc1)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #283203
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C1CCCN1C(=O)C1CCCN1C(=O)CC1C=Cc2ccccc21
Reaction #290543
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)CN(CC(O)C(Cc1ccc(OCCCN2CCSC2)cc1)NC(=O)OC1COC2OCCC12)S(=O)(=O)c1ccc2c(c1)OCO2
Reaction #291083
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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