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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55014생성일: 2026년 10월 24일

1-Bromomethyl-2,6-dichlorobenzene → 1-(2,6-Dichlorobenzyl)-3-[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazoline

https://huagongshe.com/ko/reaction/55014

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
반응물3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 22923399—
생성물1-(2,6-Dichlorobenzyl)-3-[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 2292355529%

반응 단계

The procedure similar to that described in Example 1 was repeated, except that 300 mg (0.63 mmol) of Compound 24 was used and 2,6-dichlorobenzyl bromide was used in place of methyl iodide. As a result, 117.1 mg (yield: 29%) of Compound 10 was obtained as pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624926
출처 데이터셋uspto-grants-1997_04
ORD IDord-c9f7607c9cc145cbb5f7356aba12dec0
출처 메모uspto-grants-1997_04