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1120927

CCOC(=O)C1=C(CSCCN)NC(C)=C(C(=O)OC)C1c1cccc([N+](=O)[O-])c1.O=C(O)/C=C/C(=O)O
Reaction #5745
(-)-2-(aminoethylthio)methyl-3-carboethoxy-5-carbomethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine fumarate
DOI: 10.6084/m9.figshare.5104873.v1
C1CN=C2SCCCN2C1
Reaction #165569
3,4,7,8-Tetrahydro-2H,6H-pyrimido[2,1-b]-[1,3]-thiazine
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)Nc1ccc2c(c1)N1CCCN=C1S2
Reaction #229011
DOI: 10.1039/C8SC04228D
Cl
Reaction #234416
DOI: 10.1039/C8SC04228D
Nc1ccc2c(c1)SC1=NCCCN12
Reaction #236922
DOI: 10.1039/C8SC04228D
Nc1ccc2c(c1)N1CCCN=C1S2
Reaction #266973
DOI: 10.1039/C8SC04228D
I
Reaction #272285
DOI: 10.1039/C8SC04228D
O=C1c2nc[nH]c2N(Cc2ccc(Cl)cc2)C2=NCCCN12
Reaction #323182
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2c(cc1N)N1CCCN=C1S2
Reaction #387455
DOI: 10.1039/C8SC04228D
CC(C)N1CCCN=C1SC1=C(O)CC(c2ccccc2)OC1=O
Reaction #445077
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc(SC)[nH]c1=O
Reaction #477219
product
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2ccccc2)nc(SC)[nH]c1=O
Reaction #501154
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSC1=NCCCN1.Cl
Reaction #528866
2-methylthio-1,4,5,6-tetrahydropyrimidine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NS(=O)(=O)c1cc(C2(O)CSC3=NCCCN32)cc(Cl)c1Cl
Reaction #547997
3-(3,4-Dichloro-5-sulfamoylphenyl)-3-hydroxy-2,3,6,7-tetrahydro-5H-thiazolo[3,2-a]-pyrimidine-hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NS(=O)(=O)c1cc(C2(O)CSC3=NCCCN32)ccc1Cl
Reaction #548319
3-(4-chloro-3-sulfamoylphenyl)-3-hydroxy-2,3,6,7-tetrahydro-5H-thiazolo[3,2-a]pyrimidine-hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2(O)CSC3=NCCCN32)cc1S(N)(=O)=O.Cl
Reaction #548339
3-Hydroxy-3-(4-methyl-3-sulfamoylphenyl)-2,3,6,7-tetrahydro-5H-thiazolo[3,2-a]pyrimidine-hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Br.CCSC1=NCC(O)CN1
Reaction #552279
2-(ethylthio)-1,4,5,6-tetrahydro-5-pyrimidinol, hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Br.NNC1=NCC(O)CN1
Reaction #552280
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCCN=C1SC1=C(O)CC(c2ccccc2)OC1=O
Reaction #569104
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSC1=NC(=O)C(c2ccccc2)C(=O)N1
Reaction #583486
compound
収率 34.3%DOI: 10.6084/m9.figshare.5104873.v1
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