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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 511473생성일: 2026년 10월 23일

Dimethylformamide → 3-Amino-N-methylpicolinamide

https://huagongshe.com/ko/reaction/511473

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물3-Aminopicolinic acidHCID 73836—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물Methylamine hydrochlorideHCID 6364545—
용매WaterHCID 962—
생성물3-Amino-N-methylpicolinamideHCID 1353324835.7%

반응 단계

A solution of 3-aminopicolinic acid (0.3 g, 2 mmol) in DMF (2.0 mL, 26 mmol) was cooled to 0° C., treated with DIPEA (7.57 mL, 43.4 mmol), methylamine hydrochloride (1.47 g, 21.7 mmol) and TBTU (0.837 g, 2.61 mmol). The flask was sealed and the mixture was allowed to come up to RT stirring for 3 hours. The reaction mixture was poured into water and extracted with EtOAc three times. The combined organic layers were dried over Na2SO4, filtered and concentrated to an oil which was passed through an ion exchange column (SCX). The MeOH/NH3 washes were combined to isolate 108 mg of a brown oil which crystallized upon standing. 1H NMR (400 MHz, DMSO-d6) δ 2.76 (d, J=4.80 Hz, 3H), 6.81 (br. s., 2H), 7.13 (dd, J=8.30, 1.50 Hz, 1H), 7.22 (dd, J=8.30, 4.30 Hz, 1H), 7.77 (dd, J=4.17, 1.39 Hz, 1H), 8.52 (d, J=3.79 Hz, 1H). MS (ES+): m/z=152.04 [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096624B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-3901d6d11cb64953b3f390433e7ffc5a
출처 메모uspto-grants-2015_08