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HRID 43213作成日:2026年10月23日

Diisopropylethylamine → HCID 178493464、化合物

https://huagongshe.com/ja/reaction/43213

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物2-Amino-4-diethoxymethyl-imidazole-1-carboxylic acid tert-butyl esterHCID 59292821—
反応物8-(2,6-Dichloro-3,5-dimethoxy-phenyl)quinoxaline-5-carboxylic acidHCID 59292838—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Water ethylacetateHCID 22728543—
生成物HCID 178493464HCID 17849346434.3%

反応手順

A mixture of 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid (300 mg, 0.791 mmol) (Step 179.1), 2-amino-4-diethoxymethyl-imidazole-1-carboxylic acid tert-butyl ester (226 mg, 0.791 mmol) (Step 179.8), TBTU (305 mg, 0.949 mmol, 1.2 equiv) and DIEA (409 mg, 3.17 mmol, 4 equiv) in DMF (6 mL) was stirred for 48 h at rt. After further addition of 2-amino-4-diethoxymethyl-imidazole-1-carboxylic acid tert-butyl ester (80 mg, 0.280 mmol) (Step 179.8), the reaction mixture was stirred for additional 72 h at rt, diluted with EtOAc/H2O and extracted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (EtOAc/Hex, 1:1) to afford 470 ring of a mixture of products. Part of this mixture (280 mg) was dissolved in acetone (3 mL) and H2O (2 mL) and treated with PPTS (10.9 mg). The reaction mixture was stirred for 7 h at rt, heated to 50° C., stirred for 20 h, allowed to cool to rt and diluted with EtOAc/H2O. The resulting yellow precipitate was collected by vacuum filtration and dried to provide 128 mg of the title compound: ES-MS: 472 [M+H]+; tR=4.16 min (System 1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536175B2
出典データセットuspto-grants-2013_09
ORD IDord-2aff5f40b50f4445931d7be543e15e3e
出典メモuspto-grants-2013_09