Recherche de Sous-structure

60114

CCCCC1c2cc(C(=O)O)ccc2CCN1C(=O)OC(C)(C)C
Reaction #42547
2-(tert-butoxycarbonyl)-1-butyl-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid
Rendement 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1NCCc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42548
amide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(C)NCC2
Reaction #197352
DOI: 10.1039/C8SC04228D
CC(C)CNC(=O)c1ccc2c(c1)C(C1CCCCC1)NCC2
Reaction #227149
DOI: 10.1039/C8SC04228D
CC1NCCc2ccc(C(F)(F)F)cc21
Reaction #291849
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)C1CC(NS(C)(=O)=O)CCN1CC2
Reaction #297573
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCc2ccc(C#N)cc2C1C1(c2ccccn2)CCC1
Reaction #329290
tert-Butyl 7-cyano-1-[1-(pyridin-2-yl)cyclobutyl]-3,4-dihydroisoquinoline-2(1H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2ccc(CN)cc2C1C1(c2ccccn2)CCC1
Reaction #329291
tert-Butyl 7-(aminomethyl)-1-[1-(pyridin-2-yl)cyclobutyl]-3,4-dihydroisoquinoline-2(1H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)NCc1ccc2c(c1)C(C1(c3ccccn3)CCC1)N(C(=O)OC(C)(C)C)CC2
Reaction #329292
tert-Butyl 7-{[(propylsulfonyl)amino]methyl}-1-[1-(pyridin-2-yl)cyclobutyl]-3,4-dihydroisoquinoline-2(1H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2cc(C)ccc2CCN1C(=O)C(Cl)Cl
Reaction #373752
DOI: 10.1039/C8SC04228D
CCCCC1c2cc(C(=O)O)ccc2CCN1C(=O)OC(C)(C)C
Reaction #436241
2-(tert-butoxycarbonyl)-1-butyl-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid
Rendement 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1NCCc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #436242
amide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(c1ccccc1)NCC2
Reaction #471170
7-methyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(c1ccccc1)N(C(=O)CCC(=O)O)CC2
Reaction #471171
4-(7-methyl-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-4-oxobutyric acid
Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(c1ccc3cccc-3o1)N(C)CC2.Cl
Reaction #489274
(+)-4-benzofuran-2-yl-2,7-dimethyl-1,2,3,4-tetrahydroisoquinoline, hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C(c1ccc3cccc-3s1)N(C)CC2.O=C(O)/C=C\C(=O)O
Reaction #489277
4-benzothiophen-2-yl-2,7-dimethyl-1,2,3,4-tetrahydroisoquinoline, maleate salt
DOI: 10.6084/m9.figshare.5104873.v1
CC1NCC(c2ccc(Cl)cc2)c2ccc(-c3cccnn3)cc21
Reaction #663281
4-(4-Chloro-phenyl)-7-(pyridazin-3-yl)-1-methyl-1,2,3,4-tetrahydro-isoquinoline
Rendement 57.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)NCC(c2ccc(Cl)c(Cl)c2)c2ccc(-c3ccc(N)nn3)cc21
Reaction #663284
4-(3,4-dichlorophenyl)-7-(6-aminopyridazin-3-yl)-1,1-dimethyl-1,2,3,4-tetrahydroisoquinoline
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)NCC(c2ccc(Cl)c(Cl)c2)c2ccc(-c3ccc4ncnn4c3)cc21
Reaction #663316
4-(3,4-dichlorophenyl)-7-([1,2,4]triazolo[1,5-a]pyridin-6-yl)-1,1-dimethyl-1,2,3,4-tetrahydroisoquinoline
Rendement 60.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)C1CC(NS(C)(=O)=O)CCN1CC2
Reaction #704088
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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