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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55009생성일: 2026년 10월 25일

Allyl bromide → 3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxo-1-(2-propenyl)-quinazoline

https://huagongshe.com/reaction/55009

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참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 22923399—
생성물3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxo-1-(2-propenyl)-quinazolineHCID 2292341353%

반응 단계

The procedure similar to that described in Example 1 was repeated, except that 334.6 mg (0.7 mmol) of Compound 24 was used and allyl bromide was used in place of methyl iodide. As a result, 192.8 mg (yield: 53%) of Compound 5 was obtained as pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624926
출처 데이터셋uspto-grants-1997_04
ORD IDord-7e9e21502ecf435b903a3724a8ae84d2
출처 메모uspto-grants-1997_04