子结构搜索

546909

COc1cc(/C=C2\CCCN([C@@H](C)c3ccc(F)cc3)C2=O)ccc1-n1cc(C)[n+](COP(=O)([O-])O)c1
Reaction #44597
title compound
收率 90.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44601
title compound
收率 86.3%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1CC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44614
title compound
收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@@H]1CCC(c2cc(F)c(F)c(F)c2)N1
Reaction #44661
titled compound
收率 98.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCNCC1)c1ccc(F)cc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60691
3-Chloro-N-[1-(4-fluorophenyl)-2-(piperidin-4-ylmethoxy)-ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccc(F)cc2)CC1
Reaction #60714
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccc(F)cc2)CC1
Reaction #60715
3-Chloro-N-[1-(4-fluorophenyl)-2-(1-methylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(C)SC(N[C@@H](C)c3ccc(F)cc3)=NC2=O)cc1
Reaction #74420
Methyl 4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC1=NC(=O)C(C)(c2ccc(C(=O)O)cc2)S1)c1ccc(F)cc1
Reaction #74421
4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC1=NC(=O)C(C)(c2ccc(C(=O)Cl)cc2)S1)c1ccc(F)cc1
Reaction #74422
4-(2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-4-oxo-4,5-dihydrothiazol-5-yl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC1=NC(=O)C(C)(c2ccc(C(=O)N3CCCC3)cc2)S1)c1ccc(F)cc1
Reaction #74423
2-((S)-1-(4-fluorophenyl)ethylamino)-5-methyl-5-(4-(pyrrolidine-1-carbonyl)phenyl)thiazol-4(5H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)OC(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #86486
title compound
收率 76.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cc(CNCC(F)(F)F)c(F)cc3F)CO[C@@H](CF)C[C@H]2CS1)c1ccccc1
Reaction #155590
product
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cc(CNCC(F)(F)F)c(F)cc3F)CO[C@@H](CF)C[C@H]2CS1
Reaction #155591
product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(CNCC(F)(F)F)c(F)cc2F)CO1
Reaction #155592
product
收率 106.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)CC(N)c1ccc(F)cc1
Reaction #159529
product
收率 105.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)CC(N)c1ccc(F)cc1
Reaction #159551
N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(NC(CS(N)(=O)=O)c2ccc(F)cc2)=NS(=O)(=O)C1(C)C
Reaction #159552
product
收率 34.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)(COCc1cc(C(=O)NC(C)c2ccc(F)cc2)cc(N(C)S(C)(=O)=O)c1)Cc1ccccc1
Reaction #175561
DOI: 10.1039/C8SC04228D
CN(C)C1(c2ccc(F)cc2)CCC(=CC(=O)NCCc2c[nH]c3ccccc23)CC1
Reaction #179033
DOI: 10.1039/C8SC04228D
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