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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20068생성일: 2026년 10월 23일

2,3-Diaminopyridine → tert-Butyl 4-[(2-aminopyridin-3-yl)amino]piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/20068

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DiaminopyridineHCID 9956—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,1-DichloroethaneHCID 6365—
생성물tert-Butyl 4-[(2-aminopyridin-3-yl)amino]piperidine-1-carboxylateHCID 2229321733.2%

반응 단계

Sodium triacetoxyborohydride (14.5 g, 68.7 mmol) was added to a solution of 2,3-diaminopyridine (5.00 g, 45.8 mmol) and N-(t-butoxycarbonyl)-4-piperidone (9.58 g, 48.1 mmol) in dichloroethane (75 mL) at room temperature. After 5 h, additional sodium triacetoxyborohydride was added (1.8 g) and again after another 2.5 h. The reaction was stirred overnight, and quenched with 5% aqueous sodium hydroxide. This was extracted with methylene chloride, and washed with 5% aqueous sodium hydroxide, water and saturated sodium chloride solution. After drying over sodium sulfate, the solution was filtered and evaporated to give the crude product. This was purified by chromatorgraphy (silica gel, 3 to 5% methanol in methylene chloride gradient elution), which gave the title compound (4.44 g). MS 293 (M+1) 1H NMR (500 MHz, CD3OD) δ 7.32 (dd, J=1, 5 Hz, 1H), 6.85 (dd, J=1, 8 Hz, 1H), 6.59 (dd, J=5, 8 Hz, 1H), 4.04 (d, J=13 Hz, 2H), 3.46 (m, 1H), 2.98 (br s, 2H), 2.01 (dd, J=2, 12 Hz, 2H), 1.46 (s, 9H), 1.37 (qd, J=4, 12 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ba95a0523abd4bb7b5ee1024787444d7
출처 메모uspto-grants-2010_06