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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1908744생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물2-Chloro-6-methyl-isonicotinic acid tert-butyl esterHCID 86040366—
촉매palladium(II) acetateHCID 167845—
용매Hydrochloric AcidHCID 313—
용매TetrahydrofuranHCID 8028—
생성물2-(Dimethylamino)-6-methylpyridine-4-carboxylic acidHCID 17921347—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598208B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-11044660fb2f40d5aee8ec7f0366f3e2
출처 메모uspto-grants-2013_12