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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597059생성일: 2026년 10월 26일

Dimethylformamide → Ethyl 1-(7chloroquinazolin-4-yl)-2-methyl-5-n-propoxyindol-3-ylacetate

https://huagongshe.com/reaction/597059

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrachloroethyleneHCID 31373—
반응물Ethyl 1-(7-chloroquinazolin-4-yl)-5-hydroxy-2-methylindol-3-ylacetateHCID 21449352—
생성물Ethyl 1-(7chloroquinazolin-4-yl)-2-methyl-5-n-propoxyindol-3-ylacetateHCID 21449327—

반응 단계

A solution of ethyl 1-(7-chloroquinazolin-4-yl)-5-hydroxy-2-methylindol-3-ylacetate (1.0g.) in dry dimethyl-formamide (10ml.); dried by distillation from calcium hydride, and stored over sodium alumino-silicate) was added to sodium hydride (0.068g.), and the mixture was stirred under a slight vacuum (ca 150mm. Hg) at room temperature for 15 minutes. n-Propyl iodide (0.9g.) was added to the resulting clear solution, and the mixture stirred at room temperature overnight. The solution was added to water (300ml.) and extracted with ethyl acetate (3 × 40ml.). The combined extracts were washed with a saturated solution of sodium chloride (30ml.), dried (MgSO4), and then evaporated in vacuo. The yellow oil thus obtained was treated with tetrachloroethylene (100ml.) and the solution evaporated in vacuo. This process was then replaced with ethanol (50ml.) to give ethyl 1-(7chloroquinazolin-4-yl)-2-methyl-5-n-propoxyindol-3-ylacetate as a stiff yellow syrup [NMR: 2-CH3 at 7.65 τ; pure by TLC (systems A and D)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04012513
출처 데이터셋uspto-grants-1977_03
ORD IDord-52b8c8b72f3746f799001bae010f2f45
출처 메모uspto-grants-1977_03