Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642287생성일: 2026년 10월 26일
Sodium hydride → 4-[(tert-Butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/642287
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ethyl 2-((tert-butoxycarbonyl)amino)acetate | HCID 357729 | — |
| 반응물 | 4-Bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic Acid Ethyl Ester | HCID 17951768 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-[(tert-Butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester | HCID 68427403 | 23.2% |
반응 단계
A mixture of 4-bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester (1.05 g, 2.67 mmol), tert-butoxycarbonylamino-acetic acid ethyl ester (540 mg, 2.66 mmol) and sodium hydride (60% in mineral oil, 128 mg, 3.2 mmol) in anhydrous dimethylformamide (10 mL) was stirred at 0° C. for two hours and room temperature for half an hour before it was quenched with brine. The mixture was filtered and the filtrate was extracted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow oil (319 mg): MS: (+) m/z 538.9 (M+Na+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07696223B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-21d69a1fcdb84e4cb15db075e3f583f3 |
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| 출처 메모 | uspto-grants-2010_04 |
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