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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1603006생성일: 2026년 10월 26일

Hydrochloric Acid → 2-[3-(2,6-Dichlorophenyl)ureido]-5-iodobenzoic acid

https://huagongshe.com/reaction/1603006

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzoic acid, 2-amino-5-iodo-HCID 72911—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Dichloro-2-isocyanatobenzeneHCID 604537—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물2-[3-(2,6-Dichlorophenyl)ureido]-5-iodobenzoic acidHCID 2344458759.3%

반응 단계

To an ice cooled solution of 2-amino-5-iodobenzoic acid (540 mg, 2.03 mmol) and sodium bicarbonate (170 mg, 2.03 mmol) in 9 mL of dioxane/water (2:1) was added 2,6-dichlorophenylisocyanate (468 mg, 2.44 mmol). The reaction was slowly warmed to room temperature while stirring overnight. The reaction mixture was acidified with 2N HCl and extracted with EtOAc. The product, which partially precipitated from the organic layer, was filtered and washed with EtOAc (173 mg). The filtrate was dried (MgSO4) and evaporated under reduced pressure. Trituration of the residue with Et2O afforded an additional 543 mg of 2-[3-(2,6-dichlorophenyl)ureido]-5-iodobenzoic acid: 1H-NMR (300 MHz, d6 -DMSO) δ 7.37 (t, J=8 Hz, 1H), 7.58 (d, J=8 Hz, 2H), 7.84 (dd, J=8 Hz, 4 Hz, 1H), 8.19 (d, J=4 Hz, 1H), 8.28 (d, J=8 Hz, 1H), 9.60 (s, 1H, exchangeable), 10.50 (s, 1H, exchangeable).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05985872
출처 데이터셋uspto-grants-1999_11
ORD IDord-fd94c897d4b94e37bbf90c7b3f105a4d
출처 메모uspto-grants-1999_11