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HRID 1908744作成日:2026年10月24日

Dimethylamine → 2-(Dimethylamino)-6-methylpyridine-4-carboxylic acid

https://huagongshe.com/ja/reaction/1908744

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物2-Chloro-6-methyl-isonicotinic acid tert-butyl esterHCID 86040366—
触媒palladium(II) acetateHCID 167845—
溶媒Hydrochloric AcidHCID 313—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Dimethylamino)-6-methylpyridine-4-carboxylic acidHCID 17921347—

反応手順

Under argon, a solution of 2-chloro-6-methyl-isonicotinic acid tert.-butyl ester (625 mg 2.75 mmol), Na tert.-butylate (396 mg, 4.10 mmol), Xantphos (173 mg, 0.30 mmol) and Pd(OAc)2 (83 mg, 0.37 mmol) in 2 M dimethylamine in THF (35 mL) is stirred at 110° C. for 18 h. The dark reaction mixture is cooled to rt, diluted with 6 N aq. HCl and extracted with diethyl ether (4×60 mL). The org. extracts are concentrated, the residue is dissolved in 6 N aq. HCl and heated to 100° C. for 18 h. The orange suspension is concentrated, dissolved in 1 N aq. NaOH (40 mL) and concentrated again. The residue is dissolved in 1 N aq. NaOH (3 mL) and methanol and separated by MPLC on RP-C18 silica gel to give 2-dimethylamino-6-methyl-isonicotinic acid (1.1 g) as a beige oil; LC-MS: tR=0.44 min, [M+H]+=181.07.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08598208B2
出典データセットuspto-grants-2013_12
ORD IDord-11044660fb2f40d5aee8ec7f0366f3e2
出典メモuspto-grants-2013_12