돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34910생성일: 2026년 10월 24일

Triethylamine → 4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine

https://huagongshe.com/ko/reaction/34910

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-(4-Piperidinyl)-1H-indoleHCID 702235—
반응물4-Oxo-3-thiazolidinylacetyl chlorideHCID 21297225—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물4-(3-Indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidineHCID 2129722227.5%

반응 단계

A solution of 4-oxo-3-thiazolidinylacetyl chloride (1.75 g) in tetrahydrofuran (5.00 ml) was added dropsise to a suspension of 3-(4-piperidyl)indole (2.00 g) and triethylamine (4.10 ml) in a mixture of tetrahydrofuran (15.0 ml) and chloroform (5.00 ml) at 4° to 7° C. with stirring. After the mixture was allowed to stir for 1 hour with ice-bath cooling, the resultant precipitate was removed by filtration and the solvent was evaporated in vacuo. The residue was mixed with saturated aqueous sodium hydrogen carbonate (10.0 ml) and the mixture was extracted with chloroform (20.0 ml). The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of methanol and acetone to give 4-(3-indolyl)-1-[(4-oxo-3-thiazolidinyl)acetyl]piperidine (0.92 g) as slightly brown prisms.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764514
출처 데이터셋uspto-grants-1988_08
ORD IDord-0003897d204849bf86b2e0ba626abee7
출처 메모uspto-grants-1988_08