Olcegepant, BIBN-4096, BIBN-4096BS

N-[2-[5-氨基-1(S)-[4-(4-吡啶基)哌嗪-1-甲酰基]戊基氨基]-1(R)-(3,5-二溴-4-羟基苄基)-2-氧代乙基]-4-(2-氧代-1,2,3,4-四氢喹唑啉-3-基)哌啶-1-甲酰胺Chemical Name: N-[2-[5-Amino-1(S)-[4-(4-pyridinyl)piperazin-1-ylcarbonyl]pentylamino]-1(R)-(3,5-dibromo-4-hydroxybenzyl)-2-oxoethyl]-4-(2-oxo-1,2,3,4-tetrahydroquinazolin-3-yl)piperidine-1-carboxamide
CAS No. 204697-65-4
项目整合开发状态: Phase II
项目研究机构: Boehringer Ingelheim (Originator)
合成路线:The reductive amination of 2-nitrobenzaldehyde (I) with 4-amino-1-benzylpiperidine (II) in the presence of NaBH4 gave amine (III).Subsequent hydrogenation of the nitro group of (III) over Rh/C afforded (IV),which was converted to oxoquinazoline (V) upon treatment with carbonyl diimidazole in hot DMF.Hydrogenolysis of the benzyl protecting group of (V) yielded intermediate (VI).

合成路线:Coupling of Nalpha-Cbz-Nepsilon-Boc-L-lysine (VII) with N-(4-pyridinyl)piperazine (VIII) using TBTU and HOBt afforded amide (IX).After deprotection of the carbobenzoxy group by of (IX) hydrogenation over Pd/C,the resulting amino derivative (X) was coupled with N-Fmoc-3,5-dibromo-D-tyrosine (XI) to furnish the protected dipeptide amide (XII).Removal of the Fmoc protecting group of (XII) was then achieved by treatment with diethylamine in hot MeOH yielding (XIII).After treatment of piperidinyl oxoquinazoline (VI) with carbonyl ditriazole,the resulting intermediate was coupled with amine (XIII) to produce urea (XIV).Finally,removal of the Boc group of (XIV) using trifluoroacetic acid provided the title compound.

合成路线:Condensation between 3,5-dibromotyrosine methyl ester (I) and 4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine (II) in the presence of carbonyl ditriazole (CDT) furnished the asymmetric urea (III).Subsequent hydrolysis of the ester group using LiOH provided carboxylic acid (IV).This was finally coupled with N-phenylpiperazine (V) employing O-benzotriazolyl-N,N,N',N'-tetramethyluronium tetrafluoroborate and 1-hydroxybenzotriazole to yield the corresponding amide.