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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1293538생성일: 2026년 10월 26일

Triethylamine → 1-(Benzo[1,2,3]thiadiazole-5-carbonyl)-piperidin-4-one

https://huagongshe.com/reaction/1293538

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물1,2,3-Benzothiadiazole-5-carboxylic acidHCID 2735458—
반응물4-Piperidone hydrochlorideHCID 3084851—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(Benzo[1,2,3]thiadiazole-5-carbonyl)-piperidin-4-oneHCID 2239746529.5%

반응 단계

CDI (4.5 g) added to a solution of the benzo[1,2,3]thiadiazole-5-carboxylic acid (5 g) stirring in THF (100 ml) at RT. After 1 hour 4-piperidone hydrochloride (3.7 g) and triethylamine (4.3 ml) were added and the mixture stirred overnight. The resulting mixture was diluted with ethyl acetate, washed with 2M HCl (100 ml), saturated NaHCO3 solution (200 ml) and then with saturated brine (200 ml). The organic layer was dried (MgSO4) and evaporated to leave a residue which was purified by column chromatography (silica, eluting with mixtures of ethyl acetate in dichloromethane) to give the product as a yellow oil (2.1 g; MS: APCI+(M+H)262).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07238811B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-5cbbd9b1003a49f3a3a7bfa41754bdf2
출처 메모uspto-grants-2007_07