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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452652생성일: 2026년 10월 26일

Triethylamine → 2-Phenoxy-N-[3-(4-piperidinyl) phenyl]nicotinamide

https://huagongshe.com/reaction/1452652

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Phenoxypyridine-3-carbonyl chlorideHCID 2774306—
반응물tert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylateHCID 22049268—
생성물2-Phenoxy-N-[3-(4-piperidinyl) phenyl]nicotinamideHCID 57526930—
생성물Tert-butyl 4-(3-{[(2-phenoxy-3-pyridinyl)carbonyl]amino}phenyl)-1-piperidinecarboxylateHCID 68867278—

반응 단계

A mixture of tert-butyl 4-[3-(amino)phenyl]-1-piperidinecarboxylate (0.15 mmol), 2-phenoxynicotinoyl chloride (0.23 mmol) and triethylamine (0.30 mmol) in 3 mL of solvent (CH2Cl2:THF, 1:3) was stirred at room temperature for 12 hours. The reaction mixture was purified by preparative TLC (silica, EtOAc:hexane 1:1) to afford the desired product, tert-butyl 4-(3-{[(2-phenoxy-3-pyridinyl)carbonyl]amino}phenyl)-1-piperidinecarboxylate. Trifluoroacetic acid (1.0 mL) was added to the purified product dissolved in 1.0 mL of CH2Cl2 and the solution was stirred at room temperature for 1 minute. The reaction mixture was concentrated in vacuo to afford the TFA salt of the desired product. 1H NMR (400 MHz, CDCl3) δ 9.85 (s, 1H), 8.76-8.64 (br, 1H), 8.30-8.14 (br, 1H), 7.67 (s, 1H), 7.49 (t, 2H, J=7.8 Hz), 7.42-7.29 (m, 3H), 7.24 (t, 3H, J=5.2 Hz), 7.03 (d, 1H, J=7.2 Hz), 3.59 (bd, 2H, J=11.5), 3.16-3.02 (m, 2H), 2.9-2.79 (m, 1H), 2.14-2.01 (m, 4H); ESIMS m/e: 374.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07473698B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-2d67ed583eeb4638b5ac5ba9380981ae
출처 메모uspto-grants-2009_01