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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Cyano-borohydride | HCID 498716 | — |
| 반응물 | 5-(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-N-methyl-2-nitrobenzamide | HCID 69928757 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-methyl-5-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-2-nitrobenzamide | HCID 69929569 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841289B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-17f24f06fe374049899ae91f4f06fed1 |
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| 출처 메모 | uspto-grants-2014_09 |
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