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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1683691생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 2,4-Diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridine

https://huagongshe.com/reaction/1683691

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물2,4-Diamino-6-(2,3-dihydro-3-hydroxy-2,2-dimethylbenzofuran-7-yl)pteridineHCID 19040781—
용매DichloromethaneHCID 6344—
생성물2,4-Diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridineHCID 86749513—

반응 조건

온도-60 °C

반응 단계

A stirring solution of 1.8 grams (0.011 mole) of pyridine-sulfur trioxide complex [prepared by the method of E. E. Gilbert, Chem. Rev., 62. 551-555 (1962)] in 25 mL of methylene chloride is cooled to -60° C., and a solution of 2.0 grams (0.024 mole) of dimethyl sulfoxide in 5 mL of methylene chloride is added dropwise during a 5 minute period. Upon completion of addition, the reaction mixture is stirred at -60° C. for about 10 minutes. After this time a solution of 3.2 grams (0.10 mole) of 2,4-diamino-6-(2,3-dihydro-3-hydroxy-2,2-dimethylbenzofuran-7-yl)pteridine in 10 mL of methylene chloride is added dropwise during a 5 minute period. Upon completion of addition, the reaction mixture is again stirred at -60° C. for about 10 minutes, and then 5.1 grams (0.050 mole) of triethylamine is added dropwise during a 5 minute period. The reaction mixture is then allowed to warm to ambient temperature. After this time 30 mL of water is added, and the mixture is stirred for about 10 minutes. The aqueous layer is separated and extracted with about 20 mL of methylene chloride. The extract is combined with the organic layer, and the combination is concentrated under reduced pressure, yielding 2,4-diamino-6-(2,3-dihydro-2,2-dimethyl-3-benzofuranon-7-yl)pteridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05639753
출처 데이터셋uspto-grants-1997_06
ORD IDord-84637b31d841425282564fe9eba123b6
출처 메모uspto-grants-1997_06