Recherche de Sous-structure

C(CCO)CN

CCCN(CCCCO)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2ccc(O)cc2)C(O)CNCc2cccc(OC)c2)c1
Reaction #42323
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)COC1O
Reaction #48692
desired compound
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(C)C
Reaction #48693
desired compound
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC1(F)CCCCC1
Reaction #48708
title compound
Rendement 31.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(CF)CF
Reaction #48733
desired compound
Rendement 42.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)ccc2cc1OCC(O)CN1CCC(C(O)(c2ccc(F)cc2)c2ccc(F)cc2)CC1
Reaction #50601
(±)-6-{3-[4-(bis(4-fluorophenyl)hydroxymethyl)-1-piperidinyl]-2-hydroxypropoxy}-7-methoxy-2H-1-benzopyran-2-one
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2oc(=O)c3c(c2cc1OCCCN1CCC(C(O)(c2ccc(F)cc2)c2ccc(F)cc2)CC1)CCC3
Reaction #50633
8-{3-[4-(bis(4-fluorophenyl)hydroxymethyl)-1-piperidinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](N)[C@H](OC)C2)cnc1C
Reaction #72050
title compound
Rendement 74.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cnc(C)c(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCN(Cc2ccccc2)C(C)C1=O
Reaction #73358
(±)-1-Benzyl-2-methyl-3-oxo-piperidine-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1c2nc[nH]c(=O)c2CCN1Cc1ccccc1
Reaction #73359
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cccc(C(=O)OC)c3)cn2)C1
Reaction #88183
(R)-methyl 3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)benzoate
Rendement 74.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cccc(C(=O)O)c3)cn2)C1
Reaction #88184
(R)-3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)benzoic acid
Rendement 92.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cc(C(=O)O)ccc3F)cn2)C1
Reaction #88197
(R)-3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)-4-fluorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cc(C(=O)O)ccc3OC)cn2)C1
Reaction #88198
(R)-3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)-4-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cccc(C(=O)O)c3OC)cn2)C1
Reaction #88201
(R)-3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)-2-methoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1O[C@@H]1CCCN(c2ncc(C(=O)NCc3cc(C)cc(C(=O)O)c3)cn2)C1
Reaction #88204
(R)-3-((2-(3-(2-ethoxyphenoxy)piperidin-1-yl)pyrimidine-5-carboxamido)methyl)-5-methylbenzoic acid
Rendement 71.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](O)[C@@H](CNC(=O)N(C)N=O)O2)c(=O)[nH]c1=O
Reaction #93937
white fine needles
Rendement 70.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](COCc2ccccc2)C[C@H]1CO)c1ccccc1
Reaction #155595
product
Rendement 63.8%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](C)NCc1ccc(F)c([C@]23CO[C@@H](c4cnn(C)c4)C[C@H]2CSC(N)=N3)c1
Reaction #155619
product
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant