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HRID 1291776作成日:2026年10月26日

Triethylamine → N-methoxyethoxyacetyl-(L)-valine tert-butyl ester

https://huagongshe.com/reaction/1291776

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(2-Methoxyethoxy)acetic acidHCID 27642—
反応物Diethyl cyanophosphonateHCID 76257—
反応物tert-Butyl L-valinateHCID 114626—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-methoxyethoxyacetyl-(L)-valine tert-butyl esterHCID 8070703281.2%

反応手順

At 0°, 6.4 ml (45.7 mmol) of triethylamine are added to a solution of 5 g (23.9 mmol) of (L)-valine tert-butyl ester, 2.91 g (21.7 mmol) of 2-(methoxyethoxy)-acetic acid and 3.55 g (21.7 mmol) of cyanophosphonic acid diethyl ester in 30 ml of DMF and the mixture is then stirred overnight at RT. The reaction mixture is diluted with methylene chloride, washed in succession with 10% citric acid, saturated sodium hydrogen carbonate solution and saturated sodium chloride solution and, after concentration by evaporation of the organic phase, yields 5.1 g of N-methoxyethoxyacetyl-(L)-valine tert-butyl ester, which is stirred for 1 h at RT in 22 ml of a (1:1) mixture of methylene chloride and TFA. Concentration by evaporation of the reaction solution yields the title compound in the form of a colourless oil. 1H-NMR (200 MHz, CDCl3): 10.0 (s, broad, 1H), 7.62 d, broad, 1H), 4.55 (m, 1H), 4.10 (s, 2H), 3.70 (m, 2H), 3.58 (m, 2H), 3.40 (s, 3H), 2.28 (m, 1H), 0.98 (d, J=7 Hz, 3H), 0.95 (d, J=7 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05753652
出典データセットuspto-grants-1998_05
ORD IDord-6319baa8aaeb4eb9aab4cda2aff0c823
出典メモuspto-grants-1998_05