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【结 构 式】

【分子编号】28651

【品名】4-hexyl-3,3-dimethyl-2-azetidinone

【CA登记号】

【 分 子 式 】C11H21NO

【 分 子 量 】183.29388

【元素组成】C 72.08% H 11.55% N 7.64% O 8.73%

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:(III)

The condensation of ethyl isobutyrate (I) with ethanal and trimethylsilylamine in THF gives the azetidinone (III), which is treated with 4-cyanobenzoic acid succinimidyl ester (IV) in DMF yielding 3-(4-cyanobenzamido)-2,2-dimethylnonanoic acid (V). Finally, this compound is condensed with L-phenylalanine ethyl ester (VI) by means of DEC and HOBT in dichloromethane.

1 Iijima, K.; Katada, J.; Yasuda, E.; Uno, I.; Hayashi, Y.; N-[2,2-Dimethyl-3-(N-(4-cyanobenzoyl)amino)nonanoyl]-L-phenylalanine ethyl ester as a stable ester-type inhibitor of chymotrypsin-like serine proteases: Structural requirements for potent inhibition of alpha-chymotrypsin. J Med Chem 1999, 42, 2, 312.
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) 28650 ethyl 2-methylpropanoate;ethyl isobutyrate 97-62-1 C6H12O2 详情 详情
(II) 28655 Enanthic aldehyde; 1-Heptanal; Heptaldehyde; Oenanthol; Oenanthaldehyde; Enanthal; Oenanthal; Heptyl aldehyde; n-Heptaldehyde; Enanthaldehyde; Enanthole; 1-Heptaldehyde; Heptanaldehyde; n-Heptanal; Oenanthic aldehyde; n-Heptylaldehyde; Heptanal 111-71-7 C7H14O 详情 详情
(III) 28651 4-hexyl-3,3-dimethyl-2-azetidinone C11H21NO 详情 详情
(IV) 28652 4-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]benzonitrile C12H8N2O4 详情 详情
(V) 28653 3-[(4-cyanobenzoyl)amino]-2,2-dimethylnonanoic acid C19H26N2O3 详情 详情
(VI) 28654 (2S)-3-ethoxy-1-phenyl-3-buten-2-amine C12H17NO 详情 详情
Extended Information