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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43213생성일: 2026년 10월 23일

Diisopropylethylamine → HCID 178493464, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물2-Amino-4-diethoxymethyl-imidazole-1-carboxylic acid tert-butyl esterHCID 59292821—
반응물8-(2,6-Dichloro-3,5-dimethoxy-phenyl)quinoxaline-5-carboxylic acidHCID 59292838—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Water ethylacetateHCID 22728543—
생성물HCID 178493464HCID 17849346434.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536175B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2aff5f40b50f4445931d7be543e15e3e
출처 메모uspto-grants-2013_09