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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479792생성일: 2026년 10월 24일

2-Furancarbonyl chloride → Furan-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amide

https://huagongshe.com/ko/reaction/479792

반응식

참여 물질

역할이름HCID투입량
반응물2-Furancarbonyl chlorideHCID 68242—
반응물N-(1-Boc-piperidin-3-ylmethyl)anilineHCID 12972131—
용매DichloromethaneHCID 6344—
생성물Furan-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amideHCID 5397198493%

반응 단계

To a stirred suspension of N-(1-Boc-piperidin-3-ylmethyl)-aniline 4 (61.0 mg, 0.21 mmol) and piperidinomethyl polystyrene resin (60 mg) in 0.6 mL of dry CH2Cl2 was added 2-furoyl chloride (95%, 35.1 mg, 1.2 eq.) at room temperature. After being shaken at room temperature for 4 hours, the reaction mixture was passed through an aminopropyl NH2 cartridge and washed with CH2Cl2. Removal of CH2Cl2 afforded furan-2-carboxylic acid N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl amide 13 (75 mg, 93%). LRMS 285 (M-100)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06645980B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-d7366c72ee1d411e8fa52d7305432350
출처 메모uspto-grants-2003_11