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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65673생성일: 2026년 10월 24일

Ethanol → 2,3,8,9-Tetrahydro-5-(3,4,5-trimethoxyphenyl)-9-[(3,4,5-trimethoxyphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidine

https://huagongshe.com/ko/reaction/65673

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물4,5-Dihydro-2-thiazolamineHCID 15689—
반응물Tetrahydro-3,5-bis[(3,4,5-trimethoxyphenyl)methylene]-4H-pyran-4-oneHCID 2740872—
용매ChloroformHCID 6212—
생성물2,3,8,9-Tetrahydro-5-(3,4,5-trimethoxyphenyl)-9-[(3,4,5-trimethoxyphenyl)methylene]-5H,6H-pyrano[4,3-d]thiazolo[3,2-a]pyrimidineHCID 21786680—

반응 단계

A stirred solution of tetrahydro-3,5-bis[(3,4,5-trimethoxyphenyl)methylene]-4H-pyran-4-one (3.0 g, 6.5 mmole) and 2-amino-2-thiazoline (0.8 g, 7.8 mmole) in 75 ml of CHCl3 is heated at reflux for 44 hours. After cooling, the solution is filtered to remove a small amount of insoluble material. The solvent is evaporated to give an oily residue which solidifies when treated with a small amount of EtOH. The yield is 2.2 g, m.p. 166°-168°. Crystallization from 10 ml of MeCN gives 1.5 g (42%) of light yellow solid, m.p. 153°-155°. The m.p. of a sample of this material does not change when recrystallized from MeCN.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04128648
출처 데이터셋uspto-grants-1978_12
ORD IDord-21dd2336b8384ddb984830a2611bafb1
출처 메모uspto-grants-1978_12