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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458621생성일: 2026년 10월 24일

7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione → N-(1-(7-Benzyl-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-8-yl)azepan-3-yl)-4-methylbenzenesulfonamide

https://huagongshe.com/ko/reaction/458621

반응식

참여 물질

역할이름HCID투입량
반응물7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 325372—
반응물N-(Azepan-3-yl)-4-methylbenzenesulfonamideHCID 22508595—
용매2-MethoxyethanolHCID 8019—
용매TriethylamineHCID 8471—
생성물N-(1-(7-Benzyl-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-8-yl)azepan-3-yl)-4-methylbenzenesulfonamideHCID 22508573—

반응 단계

7-Benzyl-8-chloro-1,3-dimethyl-3,7-dihydropurine-2,6-dione (2A) (1.03 g, 3.40 mmol) and N-(azepan-3-yl)-4-methylbenzenesulfonamide (6B) (1.00 g, 3.73 mmol) were dissolved in 2-methoxyethanol (30 ml) and triethylamine (2.4 ml), and the mixture was heated to 120° C. for 2 days. The solvents were evaporated and the crude product was dissolved in 100 ml of EtOAc and 100 ml of water. The aqueous phase was acidified with 1M potassium hydrogen sulphate until pH=2. The organic layer was separated and extracted with 50 ml of 1M aqueous potassium hydrogen sulphate, and 50 ml of brine, and dried over sodium sulphate. The solvent was evaporated and the crude product was purified by column chromatography on silica gel using EtOAc:heptane (1:1) as the eluent. Evaporation of the solvent gave compound (6C) as a white foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192952B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-c3d53bf8551d4b14a2dee3a4e39005a7
출처 메모uspto-grants-2007_03