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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2422589생성일: 2026년 10월 26일

4-Aminobenzoic Acid → 3-Methyl-2-[4-(3-piperidin-1-ylpropoxy)phenyl]pyrido[2,3-d]-pyrimidin-4(3h)-one

https://huagongshe.com/reaction/2422589

반응식

참여 물질

역할이름HCID투입량
반응물4-Aminobenzoic AcidHCID 978—
반응물4-(3-Piperidin-1-ylpropoxy)benzaldehydeHCID 2766324—
반응물4-{3-[(3S)-3-methylpiperidin-1-yl]propoxy}benzaldehydeHCID 7379340—
반응물4-(3-Pyrrolidin-1-ylpropoxy)benzaldehydeHCID 11651573—
반응물4-[(1-Cyclopentylpiperidin-4-yl)oxy]-2-methoxybenzaldehydeHCID 86084804—
반응물4-[(1-Cyclopentyl-4-piperidinyl)oxy]benzaldehydeHCID 86624460—
반응물4-[(1-Cyclobutyl-4-piperidinyl)oxy]benzaldehydeHCID 86624461—
반응물4-[(1-Cyclobutylpiperidin-4-yl)oxy]-2-methoxybenzaldehydeHCID 86624462—
반응물6-[(1-Cyclobutylpiperidin-4-yl)oxy]nicotinaldehydeHCID 86624463—
반응물2-[(1-Cyclobutylpiperidin-4-yl)oxy]pyrimidine-5-carbaldehydeHCID 86624465—
생성물3-Methyl-2-[4-(3-piperidin-1-ylpropoxy)phenyl]pyrido[2,3-d]-pyrimidin-4(3h)-oneHCID 11639469—

반응 단계

Compounds of Examples 16 to 59 can be produced according to the method of Example 15 or a method similar to it or a combination of the method with an ordinary method, but starting from the corresponding aminobenzoic acid, amine and separately prepared aromatic aldehydes such as 4-(3-piperidin-1-ylpropoxy)benzaldehyde, 4-(3-pyrrolidin-1-ylpropoxy)benzaldehyde, 4-[(1-cyclopentyl-4-piperidinyl)oxy]benzaldehyde, 4-[(1-cyclobutyl-4-piperidinyl)oxy]benzaldehyde, 4-[(1-cyclopentylpiperidin-4-yl)oxy]-2-methoxybenzaldehyde, 4-[(1-cyclobutylpiperidin-4-yl)oxy]-2-methoxybenzaldehyde, 6-[(1-cyclobutylpiperidin-4-yl)oxy]nicotinaldehyde, 2-[(1-cyclobutylpiperidin-4-yl)oxy]pyrimidine-5-carbaldehyde, 4-{3-[(3S)-3-methylpiperidin-1-yl]propoxy}benzaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07960394B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-4e79d52b8f524476a39c9c47a8fc7d55
출처 메모uspto-grants-2011_06