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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77402생성일: 2026년 10월 23일

Formaldehyde → N-isopropyl-2-(6-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl)acetamide

https://huagongshe.com/ko/reaction/77402

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Cyano-borohydrideHCID 498716—
반응물6-(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl-N-isopropylacetamideHCID 69929498—
촉매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물N-isopropyl-2-(6-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl)acetamideHCID 6992983439.1%

반응 조건

온도130 °C

반응 단계

2-(6-(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl-N-isopropylacetamide (EXAMPLE 4A) (100 mg, 0.23 mmol) was dissolved in acetonitrile (2 mL) before addition of formaldehyde (28 mg, 0.35 mmol) and MP-cyanoborohydride (140 mg, 0.36 mmol) followed by 2 drops of acetic acid. The resulting solution was sealed in a microwave vial and heated at 130° C. for 20 minutes. Reaction mixture was then diluted with methanol before loading directly onto a 1 g SCX cartridge. The crude material was purified by SCX. The solvent was removed under reduced pressure and then re-dissolved in methanol (1 mL) and purified by preparative-HPLC. Purified sample was free-based using 500 mg SCX cartridge to afford N-isopropyl-2-(6-(5-methylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)-4-oxo-2-phenylquinazolin-3(4H)-yl)acetamide (38 mg, 0.09 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841289B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c63974b16b5b4b1a92f85b9e477cc612
출처 메모uspto-grants-2014_09