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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133565생성일: 2026년 10월 25일

Acetic Acid → (R)-3-[[N-(2-amino-5-trifluoromethylbenzoyl)glycyl]amino]-1-(2,4-dimethoxypyrimidin-5-ylmethyl)pyrrolidine

https://huagongshe.com/reaction/133565

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2,4-Dimethoxypyrimidine-5-carbaldehydeHCID 597782—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(R)-3-[[N-(2-Amino-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidineHCID 54328411—
용매TetrahydrofuranHCID 8028—
생성물(R)-3-[[N-(2-amino-5-trifluoromethylbenzoyl)glycyl]amino]-1-(2,4-dimethoxypyrimidin-5-ylmethyl)pyrrolidineHCID 69214846—

반응 조건

온도50 °C

반응 단계

(R)-3-[[N-(2-Amino-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidine (17.2 mg, 0.04 mmol) was dissolved in THF (1 mL), and 2,4-dimethoxy-5-pyrimidinecarboxaldehyde (6.7 mg, 0.04 mmol) was added to the resulting solution. Sodium triacetoxyborohydride (12.7 mg, 0.06 mmol) and glacial acetic acid (2.4 mg, 0.04 mmol) were subsequently added to the mixture. The resulting mixture was stirred at 50° C. for 24 hours and then concentrated. The residue was dissolved in dichloromethane (1 mL) and washed with a 1 M aqueous solution (1 mL) of NaOH. The organic layer was collected and concentrated, and a dichloromethane solution of 25% trifluoroacetic acid (1 mL) was added. The resulting mixture was stirred at room temperature for 1 hour and then concentrated. The obtained residue was purified by HPLC to thereby provide (R)-3-[[N-(2-amino-5-trifluoromethylbenzoyl)glycyl]amino]-1-(2,4-dimethoxypyrimidin-5-ylmethyl)pyrrolidine (Compd. No. 2175) (18.6 mg, 78%). The purity was determined by RPLC/MS (98%). ESI/MS m/e 483 (M++H, C21H25F3N6O4).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390830B1
출처 데이터셋uspto-grants-2008_06
ORD IDord-7a64db8d4f464385a275ee2fe18c2301
출처 메모uspto-grants-2008_06