돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1769596생성일: 2026년 10월 24일

3-(Chloromethyl)pyridine hydrochloride → 6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide

https://huagongshe.com/ko/reaction/1769596

반응식

참여 물질

역할이름HCID투입량
반응물3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
반응물Lithium hydrideHCID 62714—
반응물6-ethyl-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxideHCID 135795659—
용매DimethylformamideHCID 6228—
생성물6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxideHCID 2009700720%

반응 조건

온도60 °C

반응 단계

0.48 g (60 mmol) of lithium hydride is added in portions to a solution of 5.0 g (25 mmol) of 6-ethyl-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide in 250 ml of DMF. The mixture is heated at 60° C. for 15 minutes, then 4.9 g (30 mmol) of 3-picolyl chloride hydrochloride are added and the mixture is heated at 80° C. for 3 hours. It is then largely concentrated, the residue is taken up with ethyl acetate and the mixture is extracted with 10% strength hydrochloric acid. The aqueous extract is neutralised and extracted with ethyl acetate. Relatively readily volatile impurities are removed by distillation in vacuo at 100° C./0.5 mm Hg and the residue is chromatographed. 1.4 g (20%) of 6-ethyl-4-(3-pyridylmethyl)-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7(4H,6H)-dione-1-oxide are obtained as a highly viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05382585
출처 데이터셋uspto-grants-1995_01
ORD IDord-a1c5d655e4234b35a21616054a292e2a
출처 메모uspto-grants-1995_01