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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium bisulfate | HCID 516920 | — |
| 반응물 | 1,3-Thiazole-5-carbaldehyde | HCID 2773577 | — |
| 반응물 | 2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol | HCID 54358865 | — |
| 반응물 | HCID 178511851 | HCID 178511851 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | alpha-(3-Tert-butoxycarbonylaminomethylphenyl)-5-chloro-2-(thiazol-5-yl)methylamino-benzyl alcohol | HCID 69696794 | 96.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352982B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-487c39547e64462aa5b1e8b8cd8ae5f1 |
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| 출처 메모 | uspto-grants-2002_03 |
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