Recherche de Sous-structure

CCO.Cl

CCCN(CCC)C(=O)c1cc(C)cc(C(=O)N[C@@H](CC2CCCCC2)[C@H](O)CNCc2cccc(CC)c2)c1.Cl
Reaction #42554
N1-{(1S,2R)-1-(cyclohexylmethyl)-3-[(3-ethylbenzyl)amino]-2-hydroxypropyl}-5-methyl-N3,N3-dipropylisophthalamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO[Si](C)(C)C(C)(C)C)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49088
title compound
Rendement 99.9%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCO)C1(C(NC(=O)c2cccc(C(F)(F)F)c2Cl)c2ccccc2)CCCC1
Reaction #49121
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C)cc(=O)n(CCN3CCC(C)(NCc4ccc5c(c4)OCCO5)CC3)c2c1.Cl
Reaction #68055
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidin-1-yl)ethyl)-7-methoxy-4-methylquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1ccc2c(C)cc(=O)n(CCN3CCC(NCc4ccc5c(c4)OCCO5)CC3)c2c1.Cl
Reaction #68107
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-N-methyl-4-methyl-2-oxo-1,2-dihydroquinoline-7-carboxamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(CCN2CCC(NCc3ccc4c(c3)OCCO4)CC2)c2cc(C3CC3)ccc12.Cl
Reaction #68114
7-cyclopropyl-1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-4-methylquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(=O)n(CCNC2CCN(Cc3ccc4c(c3)OCCO4)CC2)c2cc(OC)ccc12.Cl
Reaction #68149
methyl 1-(2-(1-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)piperidin-4-ylamino)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinoline-4-carboxylate hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(OC)cc2c1ccc(=O)n2CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1.Cl
Reaction #68194
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-5-propionyl-1,2-dihydro-2-oxoquinoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1cc(-c2ccncc2)c2ccccc2n1CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68225
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-4-(pyridin-4-yl)quinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2(O)O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1cc(C2O[C@H](COCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)ccc1Cl)(C(C)C)C(C)C
Reaction #74465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2ccccc2n1CCCN1CCC(O)(c2ccc(Cl)c(C(F)(F)F)c2)CC1
Reaction #75169
1-[3-{4-[4-chloro-3-(trifluoromethyl)phenyl]-4-hydroxy-1-piperidinyl}propyl]-1,3-dihydro-2H-benzimidazol-2-one
Rendement 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78350
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(F)c(-c2ccc3nc(N[C@@H]4CCC[C@@H]4NC(=O)OC(C)(C)C)ncc3c2)c1Cl
Reaction #84638
tert-butyl ((1S,2R)-2-((6-(2-chloro-3-ethoxy-6-fluorophenyl)quinazolin-2-yl)amino)cyclopentyl)carbamate
Rendement 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(F)c(-c2ccc3nc(N[C@@H]4CCC[C@@H]4N)ncc3c2)c1Cl
Reaction #84639
(1R,2S)—N1-(6-(2-chloro-3-ethoxy-6-fluorophenyl)quinazolin-2-yl)cyclopentane-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO[Si](C)(C)C(C)(C)C)c(=O)c2c(C(O)c3ccc(Cl)cc3)c(Oc3cccc(Cl)c3)ncc21
Reaction #88447
3-(3-(tert-butyldimethylsilyloxy)propyl)-6-(3-chlorophenoxy)-5-((4-chlorophenyl)(hydroxy)methyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Rendement 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)n(CCCO)c(=O)c2c(Cc3ccc(Cl)cc3)c(Oc3cccc(Cl)c3)ncc21
Reaction #88448
5-(4-chlorobenzyl)-6-(3-chlorophenoxy)-3-(3-hydroxypropyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione
Rendement 26.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(COc3ccccc3)SC21)N1CCOCC1
Reaction #96108
2,2,2-trichloroethyl α-[3-phenoxymethyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(Cc1cccc(OC(F)(F)C(F)F)c1)C(O)c1cccc(Cl)c1)c1ccc(F)c2ccccc12
Reaction #177815
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cncc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #180857
DOI: 10.1039/C8SC04228D
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