참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (2S, 4S)-1-(t-butoxycarbonyl)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine | HCID 14880265 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-pyrrolidine | HCID 14880267 | 97.5% |
반응 단계
1.92 g of (2S, 4S)-1-(t-butoxycarbonyl)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine [prepared as described in step (4) above] was dissolved in 25 ml of ethyl acetate, and 26.2 ml of a 4N dioxane solution of hydrogen chloride were added to the solution, whilst ice-cooling. The mixture was then stirred at 0° to 5° C. for 2 hours and at room temperature for 30 minutes. At the end of this time, it was poured into a saturated aqueous solution of sodium bicarbonate, to make it weakly basic, and was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, to give 1.36 g of the title compound as a powder, melting at 120°-121° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05242914 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-5a57398a5c504dffb529c848afe88765 |
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| 출처 메모 | uspto-grants-1993_09 |
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