돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218080생성일: 2026년 10월 24일

Formaldehyde → 4-[5-Methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acid

https://huagongshe.com/ko/reaction/218080

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물4-[4-(4-Carboxyphenyl)-5-methylthiazol-2-yl]-piperazine-1-carboxylic acidHCID 67195578—
반응물sodium;acetic acid;acetateHCID 178476574—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물4-[5-Methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acidHCID 5980731995%

반응 단계

4-[4-(4-Carboxyphenyl)-5-methylthiazol-2-yl]-piperazine-1-carboxylic acid tort-butyl ester (0.421 mmol) was dissolved in 4M HCl in 1,4-dioxane, and stirred at room temperature for 1 h. The solvent was then removed in vacuo, and the residue 4-(5-methyl-2-piperazin-1-yl-thiazol-4-yl)-benzoic acid was suspended in methanol (10 mL) and treated with AcOH/AcONa buffer (pH ˜5.5, 5 mL), and formaldehyde (0.547 mmol). The reaction mixture was stirred at room temperature for 1 h, then treated with NaCNBH3 (0.547 mmol) and stirred at room temperature overnight. The solvent was then removed under vacuum, and the residue was purified by column chromatography to afford the title compound (0.403 mmol, 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198283B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-cfdb7a612b9f4699bda65f09077a0aa7
출처 메모uspto-grants-2012_06