部分構造検索

1118371

COCc1csc(NC(=O)c2cc(Oc3ccc(S(C)(=O)=O)cc3)cc(O[C@@H](C)CO)c2)n1
Reaction #48772
title compound
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2cc[nH]n2)c1
Reaction #48779
title compound
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2ccn(C(=O)OC(C)(C)C)n2)c1
Reaction #48780
title compound
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2cc(F)c(S(C)(=O)=O)cc2F)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48831
desired compound
収率 1.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1NCCSC1S(=O)(=O)c1ccc(Oc2ccc(-c3ccoc3)cc2)cc1
Reaction #51451
4-(4-(furan-3-yl)phenoxy)benzenesulfonyl-tetrahydro-2H-1,4-thiazine-3-carboxylic acid
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC[C@H]1COc2ccc(S(=O)(=O)C(F)(F)F)cc2O1
Reaction #67190
N-{[(2S)-7-(TRIFLUOROMETHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}ETHANAMINE
DOI: 10.6084/m9.figshare.5104873.v1
CCCNC[C@H]1COc2ccc(S(=O)(=O)C(F)(F)F)cc2O1
Reaction #67191
N-{[(2S)-7-(TRIFLUOROMETHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}PROPAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(O)cc1)C(F)(F)F
Reaction #67287
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(S(=O)(=O)C(F)(F)F)cc1
Reaction #67288
4-[(TRIFLUOROMETHYL)SULFONYL]PHENYL ACETATE
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc2c(c1)O[C@@H](CO)CO2)C(F)(F)F
Reaction #67291
[(2S)-7-(TRIFLUOROMETHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHANOL
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@H]2COc3ccc(S(=O)(=O)C(F)(F)F)cc3O2)cc1
Reaction #67292
[(2R)-7-(TRIFLUOROMETHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL 4-METHYLBENZENESULFONATE
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OCc2ccc(Cl)nn2)cc1
Reaction #70418
title compound
収率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2ccc(COc3ccc(S(C)(=O)=O)cc3)nn2)CC1
Reaction #70419
title compound
収率 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(S(C)(=O)=O)ccc1O
Reaction #70430
title compound
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #70433
Example 41
収率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cnc(N2CCC(c3ccc(COc4ccc(S(C)(=O)=O)cc4)nc3)CC2)nc1
Reaction #70442
title compound
収率 79.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(S(C)(=O)=O)ccc1OCc1ncc(C2CCN(C(=O)OC(C)(C)C)CC2)cc1C
Reaction #70449
title compound
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCc2ccc(C3CCN(C(=O)OC(C)(C)C)CC3)cn2)ccc1S(C)(=O)=O
Reaction #70450
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(n2cnc(COc3ccc(S(C)(=O)=O)cc3F)n2)CC1
Reaction #167827
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(N2CCC(n3cc(COc4ccc(S(C)(=O)=O)cc4F)c(C(F)(F)F)n3)CC2)nc1
Reaction #167855
5-Ethyl-2-(4-(4-((2-fluoro-4-(methylsulfonyl)phenoxy)methyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)piperidin-1-yl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ