Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220124생성일: 2026년 10월 25일
Cesium carbonate → 4-(4-Benzenesulfonylphenylamino)-quinazoline-6-carboxylic acid methoxymethylamide
https://huagongshe.com/reaction/220124
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 4-(Phenylsulfonyl)aniline | HCID 516666 | — |
| 반응물 | 4-Chloroquinazoline-6-carboxylic acid methoxymethylamide | HCID 86630923 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-(4-Benzenesulfonylphenylamino)-quinazoline-6-carboxylic acid methoxymethylamide | HCID 68753616 | 66.4% |
반응 단계
4-Chloroquinazoline-6-carboxylic acid methoxymethylamide (XIV-1, 550 mg), 611 mg of 4-benzenesulfonylphenylamine, 49 mg of palladium (II) acetate, 190 mg of Xant phos and 997 mg of cesium carbonate were added to 1,4-dioxane (30 ml), and the interior of a reaction vessel was replaced with a nitrogen gas, followed by stirring at 100° C. for 2.5 hours. The reaction mixture was filtrated with Celite, and water was added to the filtrate, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated sodium chloride solution, and dried over sodium sulfate. The filtrated was concentrated, and the residue was purified by silica gel column chromatography (eluting with ethyl acetate: methanol=95:5) to obtain 4-(4-benzenesulfonylphenylamino)-quinazoline-6-carboxylic acid methoxymethylamide (XI-3, 651 mg) as a pale yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08202879B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-5eab4296fb9c4af7b3fea190143cd9a9 |
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| 출처 메모 | uspto-grants-2012_06 |
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