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HRID 1750277作成日:2026年10月27日

(S)-3-Methylpiperidine → 5-bromo-7-[(4-methylphenyl)sulfonyl]-4-[(3S)-3-methylpiperidin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1750277

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-3-MethylpiperidineHCID 641100—
反応物5-Bromo-4-Chloro-7-Tosyl-7H-Pyrrolo[2,3-D]PyrimidineHCID 57750282—
反応物3-{4-[(2S)-2-Methylmorpholin-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}benzonitrileHCID 72706904—
生成物5-bromo-7-[(4-methylphenyl)sulfonyl]-4-[(3S)-3-methylpiperidin-1-yl]-7H-pyrrolo[2,3-d]pyrimidineHCID 86706938—

反応手順

5-Bromo-4-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (P3) was reacted with the hydrochloride salt of (3S)-3-methylpiperidine according to the method described for preparation of 3-{4-[(2S)-2-methylmorpholin-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}benzonitrile (6) in Example 6. In this case, purification was effected via silica gel chromatography (Eluent: 5:1 petroleum ether/ethyl acetate), providing the product as a white solid. Yield: 4.3 g, 9.6 mmol, 92%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09156845B2
出典データセットuspto-grants-2015_10
ORD IDord-fbe80560e72d44b58d74b7d688d41ba9
出典メモuspto-grants-2015_10