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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77379생성일: 2026년 10월 26일

Formaldehyde → N-methyl-5-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-2-nitrobenzamide

https://huagongshe.com/reaction/77379

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Cyano-borohydrideHCID 498716—
반응물5-(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-N-methyl-2-nitrobenzamideHCID 69928757—
촉매Acetic AcidHCID 176—
용매AcetonitrileHCID 6342—
생성물N-methyl-5-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-2-nitrobenzamideHCID 6992956948.3%

반응 조건

온도130 °C

반응 단계

5-(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-N-methyl-2-nitrobenzamide (1.78 g, 6.13 mmol) (Intermediate 10B) was dissolved in acetonitrile (45 mL) before addition of formaldehyde (0.6 g, 7.36 mmol) and MP-cyanoborohydride (3.6 g, 9.25 mmol) followed by 6 drops of acetic acid. The resulting mixture was split into 3 microwave vials and heated at 130° C. for 20 minutes. The reaction mixture was filtered and concentrated. The resultant crude material was purified by a 50 g silica column in 100% dichloromethane, 20% methanol in dichloromethane, 100% methanol (Biotage Snap cartridge). Fractions of the product were combined and reduced to dryness under reduced pressure to afford N-methyl-5-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-2-nitrobenzamide (900 mg, 2.96 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841289B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-17f24f06fe374049899ae91f4f06fed1
출처 메모uspto-grants-2014_09