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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479236생성일: 2026년 10월 26일

Sodium hydride → [Rac]-3-{7-[2-(4-tert-butyl-phenyl)-5-methyl-oxazol-4-ylmethoxy]-benzo[b]thiophen-4-yl}-2-ethoxy-propionic acid methyl ester

https://huagongshe.com/reaction/479236

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Phosphorus oxychlorideHCID 24813—
반응물4-tert-ButylbenzaldehydeHCID 70324—
반응물2-(4-Tert-butyl-phenyl)-4-chloromethyl-5-methyl-oxazoleHCID 12158218—
반응물[Rac]-2-ethoxy-3-(7-hydroxy-benzo[b]thiophen-4-yl)-propionic acid methyl esterHCID 68616696—
용매DimethylformamideHCID 6228—
생성물[Rac]-3-{7-[2-(4-tert-butyl-phenyl)-5-methyl-oxazol-4-ylmethoxy]-benzo[b]thiophen-4-yl}-2-ethoxy-propionic acid methyl esterHCID 69556901—

반응 단계

In analogy to the procedure described in example 108 c], [rac]-2-ethoxy-3-(7-hydroxy-benzo[b]thiophen-4-yl)-propionic acid methyl ester (example 151 a]) was treated with 4-chloromethyl-2-(4-tert-butyl-phenyl)-5-methyl-oxazole (prepared from 4-tert-butyl-benzaldehyde and diacetyl monoxyme followed by treatment with POCl3 in analogy to the procedures described in examples 21 a] and b]) and sodium hydride in N,N-dimethylformamide to yield [rac]-3-{7-[2-(4-tert-butyl-phenyl)-5-methyl-oxazol-4-ylmethoxy]-benzo[b]thiophen-4-yl}-2-ethoxy-propionic acid methyl ester, which was further saponified in analogy to the procedure described in example 91 e] to yield [rac]-3-{7-[2-(4-tert-butyl-phenyl)-5-methyl-oxazol-4-ylmethoxy]-benzo[b]thiophen-4-yl}-2-ethoxy-propionic acid as colorless amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06642389B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-6d980d235d4c430ea46168f2094ac150
출처 메모uspto-grants-2003_11