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HRID 222532作成日:2026年10月25日

Water → 2-Ethoxy-2-oxoethyl 2-butyl-4-chloro-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylate

https://huagongshe.com/reaction/222532

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl bromoacetateHCID 7748—
反応物Potassium CarbonateHCID 11430—
反応物2-Butyl-4-chloro-1-({2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl}methyl)-1H-imidazole-5-carboxylic acidHCID 46783205—
溶媒DimethylformamideHCID 6228—
生成物2-Ethoxy-2-oxoethyl 2-butyl-4-chloro-1-{[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylateHCID 67979259—

反応手順

Ethyl bromoacetate (263 μL, 2.37 mmol) was added to a solution of 2-butyl-4-chloro-1-{[2′-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylic acid (Intermediate 4, 1000 mg, 1.48 mmol), and potassium carbonate (347 mg, 2.51 mmol) in N,N-dimethylformamide (10 mL). The solution was stirred for 2 hours at room temperature. Water was added and the solution was extracted with diethyl ether (2×). The organic layers were dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was used crude in the following step. LC-MS: m/z 787.1 (M+Na).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207208B2
出典データセットuspto-grants-2012_06
ORD IDord-2c65c30e3144420a9838a899de989c67
出典メモuspto-grants-2012_06