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HRID 1945641作成日:2026年10月25日

Acetic Acid → 2-{1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]azetidin-3-yl}propan-2-ol

https://huagongshe.com/reaction/1945641

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Trimethyl orthoformateHCID 9005—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-Azetidin-3-yl-propan-2-olHCID 53249204—
反応物(2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehydeHCID 59605819—
溶媒1,2-DichloroethaneHCID 11—
生成物2-{1-[2-(2-Chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)ethyl]azetidin-3-yl}propan-2-olHCID 5960565123%

反応手順

To a solution of (2-chloro-9-methyl-6-morpholin-4-yl-9H-purin-8-yl)acetaldehyde (300 mg, 1.01 mmol) in DCE (20 mL) was added 2-azetidin-3-ylpropan-2-ol (118 mg, 1.02 mmol), trimethyl orthoformate (1.11 mL, 10.14 mmol) and acetic acid (0.06 mL, 1.01 mmol). The reaction mixture was stirred at room temperature for 6 h, sodium triacetoxyborohydride (323 mg, 1.52 mmol) was added and the resulting mixture stirred for a further 18 h. The reaction mixture was loaded onto an Isolute® SCX-2 cartridge, the cartridge was washed with MeOH then the desired product eluted with 2 M NH3 in MeOH. The resulting residue was purified by column chromatography (Si—PCC, 0-10% MeOH in DCM) to give the title compound as a pale yellow oil (90 mg, 23%). LCMS (Method A): RT=2.37 min, [M+H]+ 395.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394796B2
出典データセットuspto-grants-2013_03
ORD IDord-91e9b48b1f0b4580807a4e51b114359f
出典メモuspto-grants-2013_03