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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539280생성일: 2026년 10월 24일

Ammonia → 5'-Methylspiro[chromane-4,2'-imidazole]-4',6-diamine

https://huagongshe.com/reaction/539280

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물L-HydroxyprolineHCID 5810—
반응물Potassium CarbonateHCID 11430—
반응물6-Bromo-5'-methylspiro[chromane-4,2'-imidazol]-4'-amineHCID 67979605—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물5'-Methylspiro[chromane-4,2'-imidazole]-4',6-diamineHCID 6797940765.7%

반응 단계

A mixture of 6-bromo-5′-methylspiro[chroman-4,2′-imidazol]-4′-amine (Intermediate 4, 115 mg, 0.39 mmol), trans-4-hydroxy-L-proline (51 mg, 0.39 mmol), CuI (37 mg, 0.20 mmol), and K2CO3 (162 mg, 1.17 mmol) in DMSO (0.9 mL) was stirred at r.t. for 15 min. Ammonia, (30-33% in H2O, 0.37 mL, 5.86 mmol) was added and the mixture was subjected to microwave irradiation at 110° C. for 3 h. The mixture was diluted with DMSO and water and filtered through a pad of diatomaceous earth. NaCl (s) was added and the aqueous mixture was extracted with EtOAc (5×35 mL). The combined organic phases were dried (Na2SO4) and evaporated to give a crude product which was purified by flash chromatography (4 g silica, eluent: CHCl3/(MeOH/NH3) gradient) affording the title compound (59 mg, 65% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.76-1.92 (m, 2 H), 2.19 (s, 3 H), 4.18-4.34 (m, 2 H), 4.45 (br. s., 2H), 5.69 (d, 1 H), 6.35 (dd, 1 H), 6.45 (br. s., 2 H), 6.50 (d, 1 H); MS (ES−) m/z 231 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865911B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-e8737551b14e47c5a95bf71821eb6a94
출처 메모uspto-grants-2014_10