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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1956704생성일: 2026년 10월 25일

3-Butoxy-4-(1,1-dimethylpropylamino)-cyclobut-3-ene-1,2-dione → 3-{[2-(1.1-Dimethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-methyl}-5-methyl-benzonitrile

https://huagongshe.com/reaction/1956704

반응식

참여 물질

역할이름HCID투입량
반응물3-Butoxy-4-(1,1-dimethylpropylamino)-cyclobut-3-ene-1,2-dioneHCID 15838837—
반응물3-Cyano-5-methylbenzylamineHCID 17819344—
용매TetrahydrofuranHCID 8028—
생성물3-{[2-(1.1-Dimethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-methyl}-5-methyl-benzonitrileHCID 1866364767%

반응 단계

A solution of 3-butoxy-4-(1,1-dimethyl-propylamino)cyclobut-3-ene-1,2-dione (1.44 g, 6.0 mmol, Example 3) and 3-cyano-5-methylbenzylamine from Example 7, Step 3 (6.0 mmol) and tetrahydrofuran (15 mL) were stirred at room temperature for approximately 20 hours. An additional 7 mL of tetrahydrofuran were added and stirring continued for an additional 48 hours. The solvent was removed and the residue was recrystallized twice from methanol to provide 1.251 g (67%) of the title compound as a white solid: mp 231°-133° C. (softens 229° C.); 1H NMR (DMSO-d6) δ7.78 (m, 1H), 7.62 (m, 2H), 7.51 (s, 1H), 7.41 (s, br, 1H), 4.74 (d, 2H), 2.35 (s, 3H), 1.67 (m, 2H), 1.30 (s, 6H), 0.82 (m, 3H) ppm. IR (KBr): 3290, 2240, 1780, 1670 cm-1 ; MS (m/z) 311 (M+). HPLC indicates a major component (99.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05780505
출처 데이터셋uspto-grants-1998_07
ORD IDord-8cd870d3a4b749c99e4362d4e9071143
출처 메모uspto-grants-1998_07