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HRID 74843作成日:2026年10月26日

Sodium Methoxide → 3-{4-(Cholestan-3beta-yl-oxymethyl)-[1,2,3]triazol-1-yl}propyl alpha-D-mannopyranosyl-(1->3)-alpha-D-mannopyranosyl-(1->3)-alpha-D-mannopyranoside

https://huagongshe.com/reaction/74843

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium MethoxideHCID 10942334—
反応物3-{4-(Cholestan-3beta-yl-oxymethyl)-[1,2,3]triazol-1-yl}propyl 2,3,4,6-tetra-O-benzoyl-alpha-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzoyl-alpha-D-mannopyranosyl-(1->3)-2,4,6-tri-O-benzoyl-alpha-D-mannopyranosideHCID 86658280—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物3-{4-(Cholestan-3beta-yl-oxymethyl)-[1,2,3]triazol-1-yl}propyl alpha-D-mannopyranosyl-(1->3)-alpha-D-mannopyranosyl-(1->3)-alpha-D-mannopyranosideHCID 86658283—

反応手順

The perbenzoate 58 (70 mg, 0.0341 mmol) was dissolved in anhydrous THF (2 mL) and MeOH (2 mL). The mixture was treated with a solution of 11M NaOMe in MeOH (0.2 mL, 2.2 mmol). After stirring at r.t for 2 days, the white suspension was neutralized by addition of AG50WX8 resin (H+ form). The clear solution was separated from the resin by filtration. The resin was washed with MeOH (3×2 mL). The combined filtrate and washings were evaporated to dryness and dried in vacuum dessicator under P2O5 o/n to give the polyol 59, used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828952B2
出典データセットuspto-grants-2014_09
ORD IDord-ab67d2393c92437387dc13f608bb0089
出典メモuspto-grants-2014_09