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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1248965생성일: 2026년 10월 26일

Sulfapyridine → Homosulphasalazine

https://huagongshe.com/reaction/1248965

반응식

참여 물질

역할이름HCID투입량
반응물SulfapyridineHCID 5336—
반응물(2-Hydroxyphenyl)acetic acidHCID 11970—
반응물Sodium HydroxideHCID 14798—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물HomosulphasalazineHCID 192035—

반응 단계

12 g sulfapyridine was dissolved with cooling to 0° C. in 40 ml water and 12 ml conc. hydrochloric acid. 3.5 g sodium nitrite in 20 ml water was added to the sulfapyridine solution during about 15 minutes with stirring and cooling. The diazonium salt solution was added to 7.6 g 2-hydroxy-benzeneacetic acid and 7 g sodium hydroxide in 50 ml water at 0°-10° C. After stirring for 1.5 h the solution was acidified by hydrochloric acid. The precipitating product was filtered off and washed with water. Yield 18.1 g. The product was dissolved in acetic acid and treated with 5 g decolourizing coal. The solution was filtered and evaporated in vacuum. This was repeated once, a pure product being obtained, which during partial melting at about 135° C. was converted into another crystal modification of melting point 185°-187° C. with decomposition.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04628083
출처 데이터셋uspto-grants-1986_12
ORD IDord-e64b64b6fc094a41b0a7b76a6ba35ead
출처 메모uspto-grants-1986_12