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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1361763생성일: 2026년 10월 24일

Dimethylformamide → 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide

https://huagongshe.com/ko/reaction/1361763

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Thionyl ChlorideHCID 24386—
반응물1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—
반응물2-Amino-4-(2-furyl)-5-morpholinothiazoleHCID 23144158—
용매DichloromethaneHCID 6344—
생성물1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamideHCID 23144107100%

반응 단계

1-Benzyloxycarbonylpiperidine-4-carboxylic acid (5.00 g, 19.0 mmol) was dissolved in dichloromethane (80 mL), and thionyl chloride (6.93 mL, 95.0 mmol) and DMF (0.15 mL, 1.90 mmol) were added thereto, followed by 178, stirring under heating and reflux for 3 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in dichloromethane (2 mL). The resulting solution was added to a solution of 2-amino-4-(2-furyl)-5-morpholinothiazole (2.01 g, 8.00 mmol) in pyridine (32 mL) obtained in Step 1 of Example 29, and then N,N-dimethylaminopyridine (97.6 mg, 0.800 mmol) was added thereto, followed by stirring at room temperature for 1 hour. The solvent was distilled away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:1 to 1:3) to afford the entitled Compound 43 (4.96 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07880013B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-05269a2bfa5d4b82be07e7e2f726a143
출처 메모uspto-grants-2011_02