部分構造検索

COC1(OC)CCNCC1.Cl

CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44022
mixture
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(CO)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44023
mixture
収率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC2(CC(COC(=O)N(C)C)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #44024
112
収率 136.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)OCC1c2cn[nH]c2CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44043
(5-(4-Chlorophenylsulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-4-yl)methyl dimethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCNCC1.Cl
Reaction #49263
4,4-dimethoxypiperidine hydrochloride
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCC(=O)CC2)c2c(C)c(C)n(-c3ccc(Cl)cc3Cl)c2n1
Reaction #51824
1-(2,4-dichlorophenyl)-4-(4-oxopiperidin-1-yl)-2,3,6-trimethyl-1H-pyrrolo[2,3-b]pyridine
収率 81.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #93665
N-dichloroacetylpiperid-4-one ethylene ketal
収率 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1COC2(CCN(C(=O)C(Cl)Cl)CC2)O1
Reaction #93666
N-dichloroacetyl-piperid-4-one propylene ketal
収率 66.6%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cnc(N2CCC3(CC2)OCCO3)nc1
Reaction #155972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(c2ncc(Cl)cn2)CC1
Reaction #155975
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Br)ccc1OCC1COC2(CCN(CCc3ccccc3)CC2)O1
Reaction #164518
product
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ncc(COCC2COC3(CCN(CCc4ccccc4)CC3)O2)s1
Reaction #164520
2-(2-chloro-5-thiazolyl)methoxymethyl-8-phenethyl-1,4-dioxa-8-azaspiro[4,5]decane
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(N2CCC3(CC2)OCC(Cn2nnc4ccccc42)O3)n1
Reaction #164523
2-(benzotriazol-1-yl)methyl-8-(4,6-dimethoxy-pyrimidin-2-yl)-1,4-dioxa-8-azaspiro[4,5]decane
DOI: 10.6084/m9.figshare.5104873.v1
CN(c1cc(Cl)ccc1F)C1COC2(CCN(Cc3cnc(Cl)s3)CC2)O1
Reaction #164525
N-(5-chloro-2-fluorophenyl)-N-{8-(2-chloro-5-thiazolyl)methyl-1,4-dioxa-8-aza-spiro[4,5]dec-2-yl}methanamine
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCC3(CC2)OCCO3)ccc1Cl
Reaction #174818
DOI: 10.1039/C8SC04228D
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #198568
DOI: 10.1039/C8SC04228D
Clc1ccc(Nc2cc(N3CCC4(CC3)OCCO4)nc(N3CCN(Cc4ccccc4)CC3)n2)cc1Cl
Reaction #199738
DOI: 10.1039/C8SC04228D
CC(C)N(c1nc(Cl)nc(N2C(C)(C)CC3(CC2(C)C)OCCO3)n1)C(C)C
Reaction #213690
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC2(CC(CC)N1S(=O)(=O)c1ccc(Cl)cc1)OCCO2
Reaction #226296
DOI: 10.1039/C8SC04228D
O=C1CCN(S(=O)(=O)c2ccc(CNC(=O)c3ccc(Cl)cc3)cc2)CC1
Reaction #233794
DOI: 10.1039/C8SC04228D
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