関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tert-Butylamine | HCID 6385 | — |
| 反応物 | Ethylmorpholine | HCID 7525 | — |
| 反応物 | Isobutyl chloroformate | HCID 62365 | — |
| 反応物 | (R)-3-((Benzyloxy)carbonyl)thiazolidine-4-carboxylic acid | HCID 11119045 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(benzyloxycarbonyl)-N-tert.butyl-4(R)-thiazolidinecarboxamide | HCID 18648273 | 88.6% |
反応手順
A solution of 2.67 g of N-benzyloxycarbonyl-4(R)-thiazolidinecarboxylic acid in 42 ml of dry tetrahydrofuran was stirred and cooled to -15° C. in an ice/salt bath while there were added 1.15 g of N-ethylmorpholine followed after 2 minutes by 1.87 g of isobutyl chloroformate. After a further 3 minutes 0.73 g of tert.butylamine was added dropwise and the mixture was then allowed to warm to room temperature and was stirred overnight. Tetrahydrofuran was removed by evaporation under reduced pressure and the residue was dissolved in dichloromethane. The solution was washed in sequence with water, 10% citric acid solution, water, saturated sodium bicarbonate solution and water, then dried over anhydrous sodium sulphate, filtered and evaporated to give 2.85 g of 3-(benzyloxycarbonyl)-N-tert.butyl-4(R)-thiazolidinecarboxamide as a solid which melted at 96°-98° C. after recrystallization from diethyl ether/n-hexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05620987 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-1f89d22ddfca4c4eb98f2b8f40ae0506 |
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| 出典メモ | uspto-grants-1997_04 |
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