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【结 构 式】

【分子编号】45022

【品名】ethyl 2-[(3S,5R)-3-[(tert-butoxycarbonyl)amino]-5-methyl-2-oxopyrrolidinyl]acetate

【CA登记号】

【 分 子 式 】C14H24N2O5

【 分 子 量 】300.35504

【元素组成】C 55.99% H 8.05% N 9.33% O 26.63%

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:(XVII)

Pyrrolidinone (X) was alkylated with ethyl bromoacetate to afford ester (XVII), which was further hydrolyzed to acid (XVIII). Its coupling with amino ester (XIX) in the presence of EDC and HOBt furnished amide (XX). The N-Boc group of (XX) was then cleaved with HCl in EtOAc to provide amine (XXI) Aldehyde (XXVI) was obtained by condensation of 2-aminopyridine-3-carboxaldehyde (XXII) with pyruvaldehyde dimethyl acetal (XXIII), followed by partial hydrogenation of the resulting naphthyridine (XXIV) and acid hydrolysis of the dimethyl acetal group. Finally, reductive condensation of amine (XXI) with aldehyde (XXVI) in the presence of sodium triacetoxyborohydride yielded the title compound.

2 Duggan, M.E.; Hartman, G.D.; Hoffman, W.F.; Meissner, R.S.; Perkins, J.J.; Askew, B.C.; Coleman, P.J.; Hutchinson, J.H.; Naylor-Olsen, A.M. (Merck & Co., Inc.); Integrin antagonists. EP 0934305; US 5981546; WO 9808840 .
1 Nakanishi, T.; Otsuka, T.; Hashimoto, S.; Okamoto, M.; Muramatsu, Y.; Hino, M.; Hatanaka, H.; WF14865A and B, new cathepsins B and L inhibitors produed by Aphanoascus fulvescens. I. Taxomy, production, purification and biological properties. J Antibiot 2000, 53, 5, 449.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 45015 tert-butyl (3S,5R)-5-methyl-2-oxopyrrolidinylcarbamate C10H18N2O3 详情 详情
(XVII) 45022 ethyl 2-[(3S,5R)-3-[(tert-butoxycarbonyl)amino]-5-methyl-2-oxopyrrolidinyl]acetate C14H24N2O5 详情 详情
(XVIII) 45023 2-[(3S,5R)-3-[(tert-butoxycarbonyl)amino]-5-methyl-2-oxopyrrolidinyl]acetic acid C12H20N2O5 详情 详情
(XIX) 16297 ethyl (3S)-3-amino-4-pentynoate C7H11NO2 详情 详情
(XX) 45024 ethyl (3S)-3-[(2-[(3S,5R)-3-[(tert-butoxycarbonyl)amino]-5-methyl-2-oxopyrrolidinyl]acetyl)amino]-4-pentynoate C19H29N3O6 详情 详情
(XXI) 45025 ethyl (3S)-3-([2-[(3S,5R)-3-amino-5-methyl-2-oxopyrrolidinyl]acetyl]amino)-4-pentynoate C14H21N3O4 详情 详情
(XXII) 45026   C6H6N2O 详情 详情
(XXIII) 25433 1,1-dimethoxyacetone 6342-56-9 C5H10O3 详情 详情
(XXIV) 45027 methoxy([1,8]naphthyridin-2-yl)methyl methyl ether; 2-(dimethoxymethyl)[1,8]naphthyridine C11H12N2O2 详情 详情
(XXV) 45028 methoxy(5,6,7,8-tetrahydro[1,8]naphthyridin-2-yl)methyl methyl ether; 7-(dimethoxymethyl)-1,2,3,4-tetrahydro[1,8]naphthyridine C11H16N2O2 详情 详情
(XXVI) 45029 5,6,7,8-tetrahydro[1,8]naphthyridine-2-carbaldehyde C9H10N2O 详情 详情
Extended Information