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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260800생성일: 2026년 10월 26일

(R)-3,3-Dimethyl-2-aminobutane → (+)-(R)-4-[3,4-dioxo-2-(1,2,2-trimethyl-propylamino)-cyclobut-1-enylamino]-3-ethylbenzonitrile

https://huagongshe.com/reaction/260800

반응식

참여 물질

역할이름HCID투입량
반응물(R)-3,3-Dimethyl-2-aminobutaneHCID 5324845—
반응물4-(2-Ethoxy-3,4-dioxo-cyclobut-1-enylamino)-3-ethylbenzonitrileHCID 19972918—
용매EthanolHCID 702—
생성물(+)-(R)-4-[3,4-dioxo-2-(1,2,2-trimethyl-propylamino)-cyclobut-1-enylamino]-3-ethylbenzonitrileHCID 988377852.1%

반응 단계

4-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-3-ethylbenzonitrile (1.26 g, 4.66 mmol) and a solution of (R)-1,2,2-trimethylpropylamine (9.3 mmol) in ethanol (58 mL) were stirred at room temperature for 24 hours. The resulting yellow solution was concentrated to a yellow oil, which was dissolved in acetonitrile (20 mL) and stirred at room temperature. The yellow solid which precipitated was filtered off and rinsed with ethyl acetate to yield 0.79 g (52%) of (+)-(R)-4-[3,4-dioxo-2-(1,2,2-trimethyl-propylamino)-cyclobut-1-enylamino]-3-ethylbenzonitrile as an off-white solid: mp 235°-237° C.; [α]D25 =+68.20° (DMSO, c 0.0072); 1H NMR (DMSO-d6): δ 8.04 (br s, 1H), 8.04 (d, 1H), 7.69-7.57 (m, 3H), 4.05 (m, 1H), 2.71 (q, 2H), 1.27-1.16 (overlapping doublet and triplet, 6H), 0.91 (s, 9H). IR (KBr): 3278, 2959, 2222, 1793, 1674, 1598, 1576, 1522 cm-1 ; MS (m/z) 325 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05530025
출처 데이터셋uspto-grants-1996_06
ORD IDord-f065e4551d7d4e8ca1fab6f1c141b5c0
출처 메모uspto-grants-1996_06