TBC-3486
3(S)-(1,3-苯二二醇-5-酰)-3-[N3-[1(S)-[N,N-双(2-噻基甲基)氨甲酰]戊基]脲啶]丙酸Chemical Name: 3(S)-(1,3-Benzodioxol-5-yl)-3-[N3-[1(S)-[N,N-bis(2-thienylmethyl)carbamoyl]pentyl]ureido]propionic acid
CAS No. 247044-77-5
项目整合开发状态: Preclinical
项目研究机构: Encysive Pharmaceuticals (Originator), Schering-Plough (Licensee)
合成路线:Reductive condensation of 2-thienylmethylamine (I) with 2-thiophenecarboxaldehyde (II) in the presence of NaBH(OAc)3 provided bis(2-thienylmethyl)amine (III),which was coupled with N-Boc-2-aminohexanoic acid (IV) by means of EDC and HOBt,yielding amide (V).Acid deprotection of the Boc group of (V) then gave amine (VI).
合成路线:Treatment of 3,4-(methylenedioxy)cinnamic (VII) with SOCl2 and then with EtOH provided ethyl ester (VIII).Subsequent conjugate addition of the chiral amine (IX) to ester (VIII) in the presence of BuLi gave amino ester (X).Cleavage of benzyl and alpha-methylbenzyl protecting groups of (X) was then achieved by catalytic hydrogenolysis over Pd/C.The resulting primary amine (XI) was acylated with 4-nitrophenyl chloroformate (XII) to produce carbamate (XIII),which was condensed with amine (VI) to generate urea (XIV).Finally,basic hydrolysis of the ethyl ester of (XIV) furnished the title carboxylic acid.
合成路线:Amine (I) was treated with phosgene to produce isocyanate (II),which was coupled with ethyl 3-amino-3-(3,4-methylenedioxyphenyl)propionate (III),yielding urea (IV).Basic hydrolysis of the ethyl ester of (IV) then gave the title carboxylic acid.
📌 参考资料/链接：
参考文献标题:N,N-Disubstd.amides that inhibit the binding of integrins to their receptors
文献作者:Raju,B.G.; Scott,I.L.; Biediger,R.J.; Market,R.V.; Grabbe,V.O.; Kassir,J.M.; Kogan,T.P.; Lin,S.(Texas Biotechnology Corp.)
参考来源:US 6096773; WO 9952493; WO 9952898
📄 详细内容
合成路线:Reductive condensation of 2-thienylmethylamine (I) with 2-thiophenecarboxaldehyde (II) in the presence of NaBH(OAc)3 provided bis(2-thienylmethyl)amine (III),which was coupled with N-Boc-2-aminohexanoic acid (IV) by means of EDC and HOBt,yielding amide (V).Acid deprotection of the Boc group of (V) then gave amine (VI).
合成路线:Treatment of 3,4-(methylenedioxy)cinnamic (VII) with SOCl2 and then with EtOH provided ethyl ester (VIII).Subsequent conjugate addition of the chiral amine (IX) to ester (VIII) in the presence of BuLi gave amino ester (X).Cleavage of benzyl and alpha-methylbenzyl protecting groups of (X) was then achieved by catalytic hydrogenolysis over Pd/C.The resulting primary amine (XI) was acylated with 4-nitrophenyl chloroformate (XII) to produce carbamate (XIII),which was condensed with amine (VI) to generate urea (XIV).Finally,basic hydrolysis of the ethyl ester of (XIV) furnished the title carboxylic acid.
参考文献标题:Novel N,N-disubstituted amides that are highly potent VLA-4 antagonists
文献作者:Scott,I.L.; et al.
参考来源:219th ACS Natl Meet (March 26 2000,San Francisco) 2000,Abst MEDI 284
产品链接: CAS No. 247044-77-5››