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HRID 1445367作成日:2026年10月26日

Isopropyl Acetate → (R)-N-Methoxy-3-(4-methoxybenzyl)-N-methyl-2-oxothiazolidine-4-carboxamide

https://huagongshe.com/reaction/1445367

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl AcetateHCID 7915—
反応物4-MethylmorpholineHCID 7972—
反応物N,O-DimethylhydroxylamineHCID 14232—
反応物Pivaloyl chlorideHCID 62493—
反応物(R)-3-(4-Methoxybenzyl)-2-oxothiazolidine-4-carboxylic AcidHCID 11207876—
溶媒HeptaneHCID 8900—
生成物(R)-N-Methoxy-3-(4-methoxybenzyl)-N-methyl-2-oxothiazolidine-4-carboxamideHCID 1674259270%

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666861B2
出典データセットuspto-grants-2010_02
ORD IDord-f079e57d90744fd5929e0781bd3a0bf9
出典メモuspto-grants-2010_02