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HRID 13789作成日:2026年10月27日

4-(4-Methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochloride → 4-(1-methylpiperazin-4-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[6-(5-pyrimidinyl)pyrimidin-4-ylamino]phenyl}benzamide

https://huagongshe.com/reaction/13789

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochlorideHCID 23073545—
反応物4-Methyl-3-[6-(5-pyrimidinyl)pyrimidin-4-ylamino]anilineHCID 23145896—
生成物4-(1-methylpiperazin-4-ylmethyl)-3-trifluoromethyl-N-{4-methyl-3-[6-(5-pyrimidinyl)pyrimidin-4-ylamino]phenyl}benzamideHCID 11307533—

反応手順

This compound was prepared in the same manner as in Example 1, except that 4-methyl-3-[6-(5-pyrimidinyl)pyrimidin-4-ylamino]aniline (Reference Example 21) and 4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoyl chloride dihydrochloride (Reference Example 2) were used, and that the reaction was conducted at room temperature for 17 hours and the resulting crude crystals were washed with ethyl acetate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728131B2
出典データセットuspto-grants-2010_06
ORD IDord-9da79d7c821f49658875976c5cf997ad
出典メモuspto-grants-2010_06