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HRID 629720作成日:2026年10月26日

Methanol → tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate

https://huagongshe.com/reaction/629720

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium BicarbonateHCID 516892—
反応物Methanesulfonyl azide, trifluoro-HCID 10986786—
反応物tert-butyl (2R,5R)-5-(aminomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylateHCID 86726318—
触媒Copper SulfateHCID 24462—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylateHCID 86726323—

反応手順

To a solution of tert-butyl (2R,5R)-5-(aminomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-β-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate (1 eq.) in CH2Cl2 (0.4M) was added copper(II) sulfate (0.02 eq.) and sodium bicarbonate (1 eq.) as a solution in water (NaHCO3/CuSO4)) (1M). To that mixture was added triflic azide (3.65 eq.) as a solution in CH2Cl2 (0.4M). The heterogenous mixture was homogenized by the addition of methanol and the reaction was stirred at room temperature for 30 minutes. Upon completion by LCMS, solvents were evaporated and the evaporation residue was used as such for next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315475B2
出典データセットuspto-grants-2016_04
ORD IDord-c2ea0a96f46c46179bbcc94fdf00c96a
出典メモuspto-grants-2016_04