部分構造検索

1527

Cc1ccc(S(=O)(=O)OCC(O)Cc2cc(Cl)c3ccccc3c2OCc2ccccc2)cc1
Reaction #42218
(±)-3-[1-(benzyloxy)-4-chloro-2-naphthyl]-2-hydroxypropyl 4-methylbenzenesulfonate
収率 80.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)cc(CC(O)COS(=O)(=O)c2ccc(C)cc2)c1O
Reaction #42230
(±)-3-(5-chloro-2-hydroxy-3-methoxyphenyl)-2-hydroxypropyl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42248
(±)-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methyl azide
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2cc(Cl)ccc2OCC(=O)O)cc1Cl
Reaction #44350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc(-c2cc(Cl)ccc2OCC(=O)O)cc1Cl
Reaction #44351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1-c1cc(Nc2ccc(N)cc2)nc(N)n1
Reaction #56813
title compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(Cl)cc1-c1cc(Nc2ccc(CCCC(=O)O)cc2)nc(N)n1
Reaction #56891
title compound
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(Cl)cc1CN1CCN(S(=O)(=O)c2ccccc2)CC1
Reaction #66534
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1cccc(Cl)c1CN1CCN(C(=O)Cc2ccc(Cl)cc2)CC1
Reaction #66536
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)OC(C)(C)C)CCN1.O=C(O)C(F)(F)F
Reaction #66556
sub-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc1ccccc1
Reaction #66561
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncc(Cl)s2)ccc1Oc1ccc(Cl)cc1-c1cn[nH]c1
Reaction #74515
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1[nH]ncc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2nncs2)cc1Cl
Reaction #74529
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3ccncn3)cc2Cl)ccn1
Reaction #74535
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2ccncn2)cc1Cl
Reaction #74536
desired product
収率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)Nc3cccnn3)cc2Cl)ccn1
Reaction #74546
product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2cccnn2)cc1Cl
Reaction #74552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(c2ncns2)S(=O)(=O)c2cc(F)c(Oc3ccc(Cl)cc3-c3ccnn3C3CN(C(=O)OC(C)(C)C)C3)cc2F)c(OC)c1
Reaction #74649
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(n2nccc2-c2cc(Cl)ccc2O)C1
Reaction #74650
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #74680
colorless oil
DOI: 10.6084/m9.figshare.5104873.v1
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