참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 2-Bromothiazole | HCID 76430 | — |
| 반응물 | [2-(Methoxymethyl-carbamoyl)-ethyl]-carbamic acid tert-butyl ester | HCID 86584230 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | 2-Methylpentane | HCID 7892 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Tert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamate | HCID 69802122 | 67.1% |
반응 단계
To a solution of 2-bromothiazole (5.035 g, 30.7 mmol) in dry tetrahydrofuran (125 ml) at −78° C. under nitrogen was added a solution of n-butyllithium in hexanes (1.6 M, 17.6 ml, 28.2 mmol) over a period of 30 minutes, followed by a solution of [3-(methoxymethylamino)-3-oxopropyl]carbamic acid 1,1-dimethylethyl ester (2.976 g, 12.8 mmol) in dry tetrahydrofuran (30 ml) added over 30 minutes. The reaction mixture was allowed to warm up to 0° C., quenched with saturated ammonium chloride and extracted with ethyl acetate (3×100 ml). The combined extracts were washed with water (3×50 ml) and saturated brine solution (1×100 ml), dried (magnesium sulphate) and concentrated in vacuo to leave a crude orange oil. Flash chromatography (silica, 25% ethyl acetate in isohexane) gave 2.2 g of a pale yellow oil (67%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06887871B2 |
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| 출처 데이터셋 | uspto-grants-2005_05 |
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| ORD ID | ord-81cd7b7aae524d368ae7775492dbbe36 |
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| 출처 메모 | uspto-grants-2005_05 |
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