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HRID 27347作成日:2026年10月26日

4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester

https://huagongshe.com/reaction/27347

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物N-Benzyloxycarbonyl-beta-alanineHCID 75313—
反応物tert-Butyl L-prolinate hydrochlorideHCID 6453107—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物carbobenzoxy-beta-alanyl-L-proline t-butyl esterHCID 54135485—

反応手順

4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221706
出典データセットuspto-grants-1980_09
ORD IDord-c7cd6af73aca49feafad7a587907044d
出典メモuspto-grants-1980_09