【结 构 式】 |
【分子编号】17557 【品名】methyl (2S)-3-amino-2-[(butoxycarbonyl)amino]propanoate hydrochloride 【CA登记号】 |
【 分 子 式 】C9H19ClN2O4 【 分 子 量 】254.71364 【元素组成】C 42.44% H 7.52% Cl 13.92% N 11% O 25.13% |
合成路线1
该中间体在本合成路线中的序号:(VI)Reaction of 4-cyanobenzaldehyde (I) with hydroxylamine sulfate in methanol gives 4-cyanobenzaldoxime (II). A 1,3-dipolar cycloaddition of (II) with isobutyl vinylacetate using N-chlorosuccinimide provides the racemic isoxazoline derivative (III). Treatment of (III) with lipase PS30 selectively converts the (R)-isomer to an optically pure acid (IV). Coupling of (IV) with methyl N2-(n-butyloxycarbonyl)-L-2,3-diaminopropionate (VI), which is derived from its corresponding commerically available acid (V), gives the intermediate (VII). Treatment of (VII) with HCl in methanol and ethyl acetate followed by ammonium acetate affords DMP 754 as a crystalline product. Saponification of DMP 754 using LiOH provides the corresponding acid (VIII).
【1】 Anzalone, L.; Storace, L. Ward, R.; Kauffman, G.S.; Zhang, L.-H.; Ma, P.; The chiral specific synthesis of DMP 754, a platelet GPIIb/IIIa antagonist. Tetrahedron Lett 1996, 37, 26, 4455-8. |
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) | 17552 | 4-formylbenzonitrile; 4-Cyanobenzaldehyde | 105-07-7 | C8H5NO | 详情 | 详情 |
(II) | 17553 | 4-[(hydroxyimino)methyl]benzonitrile | C8H6N2O | 详情 | 详情 | |
(III) | 17554 | isobutyl 2-[3-(4-cyanophenyl)-4,5-dihydro-5-isoxazolyl]acetate | C16H18N2O3 | 详情 | 详情 | |
(IV) | 17555 | 2-[(5R)-3-(4-cyanophenyl)-4,5-dihydro-5-isoxazolyl]acetic acid | C12H10N2O3 | 详情 | 详情 | |
(V) | 17556 | (2S)-3-amino-2-[(butoxycarbonyl)amino]propionic acid | C8H16N2O4 | 详情 | 详情 | |
(VI) | 17557 | methyl (2S)-3-amino-2-[(butoxycarbonyl)amino]propanoate hydrochloride | C9H19ClN2O4 | 详情 | 详情 | |
(VII) | 17558 | methyl (2S)-2-[(butoxycarbonyl)amino]-3-([2-[(5R)-3-(4-cyanophenyl)-4,5-dihydro-5-isoxazolyl]acetyl]amino)propanoate | C21H26N4O6 | 详情 | 详情 | |
(VIII) | 17559 | (2S)-3-[[2-((5R)-3-[4-[amino(imino)methyl]phenyl]-4,5-dihydro-5-isoxazolyl)acetyl]amino]-2-[(butoxycarbonyl)amino]propionic acid | C20H27N5O6 | 详情 | 详情 |