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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251346생성일: 2026년 10월 26일

Iodine → 3-[5-Amino-4-(tetrahydro-pyran-4-carbonyl)-imidazol-1-yl]-N-cyclopropyl-4-methyl-benzamide

https://huagongshe.com/reaction/251346

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물TetrahydrofuranHCID 8028—
반응물MagnesiumHCID 5462224—
반응물4-BromotetrahydropyranHCID 13349654—
반응물HCID 58088961HCID 58088961—
생성물3-[5-Amino-4-(tetrahydro-pyran-4-carbonyl)-imidazol-1-yl]-N-cyclopropyl-4-methyl-benzamideHCID 2486065830%

반응 단계

A solution of 4-bromo-tetrahydro-pyran (0.82g, 5 mmol) in dry THF (10 mL) was added dropwise to the suspension of magnesium (132 mg, 5.5 mmol) and iodine (25 mg) in dry THF (20 mL) at 50° C. under N2. The mixture was stirred for 30 min after addition at 50° C., then cooled to room temperature. Then a THF (10 mL) solution of 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide (90 mg, 0.32 mmol) was added to the reaction mixture and it was stirred at room temperature for 3h then quenched with HCl (2N) and stirred at room temperature overnight. The pH of the solution was adjusted pH 8 with saturated aqueous K2CO3 was and it was extracted with EtOAc. The organic layer was washed by water and brine, dried over Na2SO4, and concentrated. The crude product was purified by column chromatography on silical gel (EtOAc˜EtOAc:MeOH:Et3N=100:10:1), and the product was obtained as a beige solid (35 mg, 30%). HPLC (4 minute gradient) tR=3.05 min; MS m/z 369.18 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863314B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-1cf12a8550e84eff861857800313f34d
출처 메모uspto-grants-2011_01