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HRID 63903作成日:2026年10月26日

2-Iodoxybenzoic acid → HCID 178477520、化合物

https://huagongshe.com/reaction/63903

反応式

関与物質

役割名称HCID仕込み量
反応物2-Iodoxybenzoic acidHCID 108794—
反応物6-bromo-1-methyl-2,4-dioxo-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidine-5-carbaldehydeHCID 118863132—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物HCID 178477520HCID 17847752057.5%

反応条件

温度50 °C

反応手順

To a solution of 6-bromo-5-(bromomethyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy) propyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (See Compound 2, Step 3, 800 mg, 1.61 mmol) in DMSO (10 mL) was added 2-iodoxybenzoic acid (541.7 mg, 1.93 mmol). The reaction was heated at 50° C. for 1.5 h, cooled to RT, diluted with water (20 mL) and extracted with EA (3×10 mL). The combined organic layers were washed with aq. NH4Cl (20 mL), dried over Na2SO4 and concentrated to a residue which was purified by chromatography eluted with PE/EA (5:1 to 1:1) to give ethyl 6-bromo-1-methyl-2,4-dioxo-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)-1,2,3,4-tetrahydro thieno[2,3-d]pyrimidine-5-carbaldehyde (400 mg, 57.5% yield) as a white solid. LCMS: [MH+-THP] 347 and TR=1.665 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447114B2
出典データセットuspto-grants-2016_09
ORD IDord-e134f5e72867454caa1bf920628872de
出典メモuspto-grants-2016_09