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HRID 1077567作成日:2026年10月27日

1-Pyrroline → Diphenyl pyrrolidine-2-phosphonate

https://huagongshe.com/reaction/1077567

反応式

関与物質

役割名称HCID仕込み量
反応物1-PyrrolineHCID 79803—
反応物L-ProlineHCID 145742—
反応物2-PhosphopyrrolidineHCID 19431371—
反応物DiphenoxyphosphanolateHCID 23418553—
反応物H-Asp-Arg-Val-Tyr-Val-His-Pro-Ala-OHHCID 178448346—
生成物Diphenyl pyrrolidine-2-phosphonateHCID 1132657849%

反応条件

温度85 °C

反応手順

This compound was synthesized from 1-pyrroline trimer (Nomura, Y., Ogawa, K., Takeuchi, Y., Tomoda, S., One Step Synthesis and Structural Confirmation with 1-Pyrroline Trimer, Chem. Lett. 1977, 693-696) and diphenyl phosphite using the procedure previously described for the synthesis of the diethyl ester (Petrillo, E. W., Spitzmiller, E. R., Synthesis of 2-Phosphopyrrolidine and Its Substitution for Proline in an Inhibitor of Angiotensin-Converting Enzyme, Tet. Lett. 1979, 51, 4929). A mixture of 1-pyrroline trimer (17 mmol, 3.5 g) and diphenyl phosphite (50 mmol, 11.7 g) was heated at 85° C. for 1.5 h under argon to give crude diphenyl pyrrolidine-2-phosphonate which was dissolved in 100 ml of dry diethyl ether, filtered and saturated with dry gaseous HCl. The precipitated hydrochloride 1 was collected by filtration, washed with ether and recrystallized from acetone, to give the pure product as a white solid in 49% yield: mp 146°-148° C.; 1H-NMR (D2O) δ(ppm): 2.0-2.5 (m, 4H), 3.40 (m, 2H), 4.25 (m, 1H), 6.90-7.30 (m, 10H); MS (FAB) m/e 304 (M-Cl)30. Anal. (C16H19NO3PCl): C, H, N, Cl.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05543396
出典データセットuspto-grants-1996_08
ORD IDord-34715100336a453da7c90c0485db0489
出典メモuspto-grants-1996_08