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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275875생성일: 2026년 10월 26일

Potassium bisulfate → alpha-(3-Tert-butoxycarbonylaminomethylphenyl)-5-chloro-2-(thiazol-5-yl)methylamino-benzyl alcohol

https://huagongshe.com/reaction/275875

반응식

참여 물질

역할이름HCID투입량
반응물Potassium bisulfateHCID 516920—
반응물1,3-Thiazole-5-carbaldehydeHCID 2773577—
반응물2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
반응물HCID 178511851HCID 178511851—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물alpha-(3-Tert-butoxycarbonylaminomethylphenyl)-5-chloro-2-(thiazol-5-yl)methylamino-benzyl alcoholHCID 6969679496.2%

반응 조건

온도60 °C

반응 단계

In methanol (10 ml) were dissolved 2-amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-chlorobenzyl alcohol (1 g) produced in Example (1) and thiazole-5-carboxyaldehyde (0.34 g). To the solution were added acetic acid (0.33 g) and cyano sodium borohydride (0.21 g). The mixture was stirred for one hour at 60° C. The reaction mixture was added to a 5% aqueous solution of potassium hydrogensulfate, followed by extraction with ethyl acetate (50 ml). The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give α-(3-tert-butoxycarbonylaminomethylphenyl)-5-chloro-2-(thiazol-5-yl)methylamino-benzyl alcohol (1.22 g) as a colorless amorphous solid product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352982B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-487c39547e64462aa5b1e8b8cd8ae5f1
출처 메모uspto-grants-2002_03