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HRID 511609作成日:2026年10月25日

Sodium cyanoborohydride → benzyl (3-((((3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)(methyl)amino)cyclobutyl)carbamate

https://huagongshe.com/reaction/511609

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium cyanoborohydrideHCID 5003444—
反応物9-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-((methylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amineHCID 11023641—
反応物Benzyl (3-oxocyclobutyl)carbamateHCID 19794323—
溶媒MethanolHCID 887—
生成物benzyl (3-((((3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl)(methyl)amino)cyclobutyl)carbamateHCID 8666611529.1%

反応手順

To a solution of 9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((methylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine (190 mg, 0.59 mmol) and benzyl (3-oxocyclobutyl)carbamate (240 mg, 1.37 mmol) in MeOH (5 mL) was added Ti[OCH(CH3)2]4 (216 mg, 0.59 mmol). The mixture was stirred at rt for 1 h. Then NaCNBH3 (95 mg, 1.52 mmol) was added, the reaction was stirred at rt overnight. The reaction was filtered and evaporated, the residue was purified by prep-TLC (DCM:MeOH=20:1) to obtain the desired compound (90 mg, yield 29%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096634B2
出典データセットuspto-grants-2015_08
ORD IDord-7ed23fc283d84dee9734e43b3e193e60
出典メモuspto-grants-2015_08