돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394318생성일: 2026년 10월 24일

Triphenylphosphine → HCID 68617831, 화합물

https://huagongshe.com/ko/reaction/394318

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-(Benzyloxy)-3-methoxybenzaldehydeHCID 75506—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Ethyl isopropoxyacetateHCID 537908—
반응물Methyl 4-bromo-3-oxopentanoateHCID 9815681—
반응물HCID 22647410HCID 22647410—
반응물668478-79-3HCID 22647568—
반응물[Rac]-3-(4-hydroxy-3-methoxy-phenyl)-2-isopropoxy-propionic acid ethyl esterHCID 68616023—
용매TetrahydrofuranHCID 8028—
생성물HCID 68617831HCID 68617831—

반응 단계

In analogy to the procedure described in example 1 d], [rac]-3-(4-hydroxy-3-methoxy-phenyl)-2-isopropoxy-propionic acid ethyl ester [prepared from isopropoxy-acetic acid ethyl ester (Tetrahedron (1982), 38(17), 2733-9) and 4-benzyloxy-3-methoxy-benzaldehyde in analogy to the procedures described in examples 54 a]to c)] was reacted with 2-[2-(3,5-dimethyl-phenyl)-5-methyl-thiazol-4-yl]-ethanol (prepared from [rac]-4-bromo-3-oxo-pentanoic acid methyl ester [PCT Int. Appl. (2001), WO 01/79202] and 3,5-dimethyl-thiobenzamide (from 3,5-dimethyl-benzonitrile and NaSH, NH4Cl in N,N-dimethylformamide) in analogy to the procedures described in examples 12 a] and 12 b]) in tetrahydrofuran in the presence of triphenylphosphine and DEAD (diethyl azodicarboxylate) to yield [rac]-3-(4-{2-[2-(3,5-dimethyl-phenyl)-5-methyl-thiazol-4-yl]-ethoxy}-3-methoxy-phenyl)-2-isopropoxy-propionic acid ethyl ester, which was farther saponified in analogy to the procedure described in example 4 e], to yield [rac]-3-(4-{2-[2-(3,5-dimethyl-phenyl)-5-methyl-thiazol-4-yl]-ethoxy}-3-methoxy-phenyl)-2-isopropoxy-propionic acid as light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809110B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-6263b24073bf4071ac6a7d7bd77b053b
출처 메모uspto-grants-2004_10