참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropyl Acetate | HCID 7915 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | (R)-3-(4-Methoxybenzyl)-2-oxothiazolidine-4-carboxylic Acid | HCID 11207876 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | (R)-N-Methoxy-3-(4-methoxybenzyl)-N-methyl-2-oxothiazolidine-4-carboxamide | HCID 16742592 | 70% |
반응 단계
A 22 L three-necked round bottom flask fitted with an internal temperature probe and a mechanical stirrer was charged with the title compound from Example 3 (310.0 g, 1.16 mol) and isopropyl acetate (2.4 L). The vessel was purged with nitrogen and cooled to 0° C. N-methylmorpholine (130.0 g, 1.29 mol) was added dropwise such that the internal reaction temperature never increased above 5° C. The reaction became cloudy. Pivaloyl chloride (150.0 g, 1.24 mol) was added dropwise such that the internal reaction temperature never increased above 5° C. The reaction was stirred at 0° C. for 45 minutes. N-methoxy-methanamine (78.0 g, 1.28 mol) was added dropwise, again keeping the internal reaction temperature below 5° C. The reaction was monitored by HPLC and was worked up when the ratio of the product to starting material was 4:1 (approximately 30 minutes after amine addition). The mixture was then washed with 0.1 M HCl and satd aq NaHCO3. The organic phase was separated and concentrated to a final volume of 1.0 L by distillation. Upon stirring, a precipitate began to form. A 250 mL portion of n-heptane was added, and the mixture was stirred vigorously. The solid was filtered and dried in a vacuum oven at 40° C. to afford the title compound (250 g, 70%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07666861B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-f079e57d90744fd5929e0781bd3a0bf9 |
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| 출처 메모 | uspto-grants-2010_02 |
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