돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1524882생성일: 2026년 10월 26일

Acetohydroxamic Acid → [(Z)-1-aminoethylideneamino] 2-fluoro-6-iodobenzoate

https://huagongshe.com/reaction/1524882

반응식

참여 물질

역할이름HCID투입량
반응물Acetohydroxamic AcidHCID 1990—
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물2-Fluoro-6-iodobenzoic acidHCID 2733302—
용매DichloromethaneHCID 6344—
생성물[(Z)-1-aminoethylideneamino] 2-fluoro-6-iodobenzoateHCID 87262981—

반응 단계

Alternately, acid (XXXa) is prepared by first converting 2-fluoro-6-iodobenzoic acid to the acid chloride by reaction with a chlorinating agent such as oxalyl chloride, in a solvent such as DCM, with a catalytic amount of DMF, at a temperature of 0° C. Subsequent reaction of the acid chloride with N-hydroxyacetamide in a solvent such as CH2Cl2 provides (Z)—N′-((2-fluoro-6-iodobenzoyl)oxy)acetimidamide. 5-(2-Fluoro-6-iodophenyl)-3-methyl-1,2,4-oxadiazole is prepared by reacting (Z)—N′-((2-fluoro-6-iodobenzoyl)oxy)acetimidamide with sodium acetate, in a solvent such as tert-butanol, at temperatures ranging from 100° C. to 110° C. 3-Fluoro-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (XXXa) is prepared by reacting 5-(2-fluoro-6-iodophenyl)-3-methyl-1,2,4-oxadiazole with a grignard reagent such as i-PrMgCl, in a suitable solvent such as THF and the like, at a temperature of −78° C. Subsequent addition of CO2 gas, at a temperature of −78° C. provides 3-fluoro-2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (XXXa).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09079911B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-35c0287771a14ac087ecf2765654b535
출처 메모uspto-grants-2015_07