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1311811

CC(=O)c1ccc(OCCCCl)cc1
Reaction #4822
p-chloropropoxy acetophenone
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)CCCOc1ccc(C(=O)c2cn3cccc(C)c3n2)cc1
Reaction #4825
title compound
Ausbeute 197.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCCCCl)cc1
Reaction #8450
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(OCCCCl)cc1F
Reaction #8460
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3F)nc2c1
Reaction #8461
2-(4′-chloropropoxy-2′fluorophenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc(OCCCCl)cc1C
Reaction #8463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCCl)ccc1C(=O)CBr
Reaction #8464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn2cc(-c3ccc(OCCCCl)cc3C)nc2c1
Reaction #8465
2-(4′-chloropropoxy-2′-methylphenyl)-7-methylimidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Br.COc1cc(-c2cn3ccc(C)cc3n2)ccc1OCCCCl
Reaction #8467
title compound
Ausbeute 70.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCCl)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49603
4-chloro-5-(3-chloropropoxy)-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)CCCOc1cc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c(c1Cl)CNC2=O
Reaction #49604
4-chloro-5-[3-[N-ethyl(2-hydroxyethyl)amino]propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCN3CCC[C@H]3CO)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49608
(S)-4-chloro-5-[3-(2-hydroxymethylpyrrolidin-1-yl)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCN3CCC(CO)CC3)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49609
4-chloro-5-[3-(4-hydroxymethylpiperidin-1-yl)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2cc(OCCCN3CCC(O)CC3)c(Cl)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49610
4-chloro-5-[3-(4-hydroxypiperidin-1-yl)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)NCCCOc1cc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c(c1Cl)CNC2=O
Reaction #49611
4-chloro-5-[3-(1-hydroxy-2-methyl-2-propylamino)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CCCOc2cc(-c3cc4cc(CN5CCCCC5)ccc4n3C(=O)OC(C)(C)C)c3c(c2Cl)CNC3=O)CC1
Reaction #49612
4-chloro-5-[3-(4-methylpyperazin-1-yl)propoxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidin-1-ylmethyl)indol-2-yl]isoindolinone
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(OCCCCl)cc1
Reaction #61972
title compound
DOI: 10.6084/m9.figshare.5104873.v1
ClCCCOc1ccc(CN2CCCCC2)cc1
Reaction #61973
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)CCN(Cc1ccc(OCCCN3CCCCC3)cc1)C2
Reaction #61980
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)=O)ccc1OCCCN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83849
1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-methoxyphenyl]-ethanone
Ausbeute 58.6%DOI: 10.6084/m9.figshare.5104873.v1
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