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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369381생성일: 2026년 10월 25일

Diiodomethane → 6-chloro-8-(3-fluorophenyl)-2-iodo-9-methyl-9H-purine

https://huagongshe.com/reaction/1369381

반응식

참여 물질

역할이름HCID투입량
반응물DiiodomethaneHCID 6346—
반응물Isoamyl NitriteHCID 8053—
반응물HCID 10492805HCID 10492805—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물6-chloro-8-(3-fluorophenyl)-2-iodo-9-methyl-9H-purineHCID 995226575%

반응 단계

6-Chloro-8-(3-fluorophenyl)-9-methyl-9H-2-purinyl-amine (960 g) was dissolved in 9.6 liters of tetrahydrofuran and then 774.3 g of cuprous iodide and 1.49 liters of diiodomethane were added thereto. Isoamyl nitrite (1.49 liters) was added dropwise during 1 hour into the mixture with heating under reflux. The reaction solution was heated under reflux for 15 minutes, cooled, diluted with 4 liters of ethyl acetate and then filtered through Celite followed by washing with ethyl acetate three times (3×2 liters). The filtrate and the washings were combined and washed with 8 liters of water and 8 liters of brine. The organic layer was dried over 2 kg of anhydrous sodium sulfate and concentrated to about 3 liters. The concentrated solution was diluted with 10 liters of hexane and the resulting crystals were filtered and washed with 1 liter of hexane. The crystals were then dried at 50° C. for 4 hours to give 1076 g of 6-chloro-8-(3-fluorophenyl)-2-iodo-9-methyl-9H-purine. The yield was 75%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579868B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-8fef669b7dc2463e96e76a0d206f45e6
출처 메모uspto-grants-2003_06