【结 构 式】 |
【分子编号】62773 【品名】2-({4-[2-(tert-butoxy)-2-oxoethoxy]benzoyl}amino)acetic acid 【CA登记号】 |
【 分 子 式 】C15H19NO6 【 分 子 量 】309.319 【元素组成】C 58.25% H 6.19% N 4.53% O 31.03% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(IX)N-Cbz-L-Valinal cyanohydrin (I) is converted into imidate (II) and then condensed with 2-aminophenol (III) to afford benzoxazole (IV). Removal of the N-Cbz group of (IV) with H2 and Pd/C provides amine (V), which is then coupled to N-Cbz-valyl proline (VI), yielding the dipeptide amide (VII). After hydrogenolysis of the N-Cbz protecting group of (VII), the free amine (VIII) is coupled to the acid fragment (IX) by means of EDC/pyridine to furnish (X).
【1】 Sato, F.; Inoue, Y.; Omodani, T.; Imano, K.; Okazaki, H.; Takemura, T.; Komiya, M.; Design and synthesis of peptide-based carboxylic acid-containing transition-state inhibitors of human neutrophil elastase. Bioorg Med Chem Lett 2002, 12, 4, 551. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 62768 | benzyl (1S)-1-[cyano(hydroxy)methyl]-2-methylpropylcarbamate | C14H18N2O3 | 详情 | 详情 | |
(II) | 62769 | ethyl (3S)-3-{[(benzyloxy)carbonyl]amino}-2-hydroxy-4-methylpentanimidoate | C16H24N2O4 | 详情 | 详情 | |
(III) | 18663 | o-aminophenol; 2-aminophenol | 95-55-6 | C6H7NO | 详情 | 详情 |
(IV) | 62770 | benzyl (1S)-1-[1,3-benzoxazol-2-yl(hydroxy)methyl]-2-methylpropylcarbamate | C20H22N2O4 | 详情 | 详情 | |
(V) | 62771 | (2S)-2-amino-1-(1,3-benzoxazol-2-yl)-3-methyl-1-butanol | C12H16N2O2 | 详情 | 详情 | |
(VI) | 22787 | (2S)-1-((2S)-2-[[(benzyloxy)carbonyl]amino]-3-methylbutanoyl)-2-pyrrolidinecarboxylic acid | C18H24N2O5 | 详情 | 详情 | |
(VII) | 62772 | benzyl (1S)-1-({(2S)-2-[({(1S)-1-[1,3-benzoxazol-2-yl(hydroxy)methyl]-2-methylpropyl}amino)carbonyl]pyrrolidinyl}carbonyl)-2-methylpropylcarbamate | C30H38N4O6 | 详情 | 详情 | |
(VIII) | 55792 | (2S)-1-[(2S)-2-amino-3-methylbutanoyl]-N-{(1S)-1-[(S)-1,3-benzoxazol-2-yl(hydroxy)methyl]-2-methylpropyl}-2-pyrrolidinecarboxamide | C22H32N4O4 | 详情 | 详情 | |
(IX) | 62773 | 2-({4-[2-(tert-butoxy)-2-oxoethoxy]benzoyl}amino)acetic acid | C15H19NO6 | 详情 | 详情 | |
(X) | 62774 | tert-butyl 2-(4-{[(2-{[(1S)-1-({(2S)-2-[({(1S)-1-[1,3-benzoxazol-2-yl(hydroxy)methyl]-2-methylpropyl}amino)carbonyl]pyrrolidinyl}carbonyl)-2-methylpropyl]amino}-2-oxoethyl)amino]carbonyl}phenoxy)acetate | C37H49N5O9 | 详情 | 详情 |
Extended Information