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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1622011생성일: 2026년 10월 23일

Hydrochloric Acid → Tert-butyl 5-amino-2-chloropyridin-3-ylcarbamate

https://huagongshe.com/ko/reaction/1622011

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Tert-butyl 2-chloro-5-(diphenylmethyleneamino)pyridin-3-ylcarbamateHCID 86647087—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl 5-amino-2-chloropyridin-3-ylcarbamateHCID 86647086—

반응 단계

To a solution of tert-butyl 2-chloro-5-(diphenylmethyleneamino)pyridin-3-ylcarbamate (0.280 g, 0.686 mmol) in THF (5 mL) was added hydrochloric acid, In (JT Baker) (0.031 mL, 1.030 mmol). The reaction was stirred at rt in closed system for 20 min. The reaction mixture was partitioned between EtOAc/sat. NaHCO3. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layer were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (24 g, 3% MeOH in DCM) to afford the desired product as a white foam-like solid (135.0 mg). MS (ESI pos. ion) m/z: 244.1. 1H NMR (300 MHz, CDCl3) δ ppm 1.54 (s, 9H) 3.73 (br. s., 2H) 6.93 (br. s., 1H) 7.52 (d, J=2.63 Hz, 1H) 7.94 (d, J=2.63 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08772480B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-8bd3a173dbf941afa14831e974a6f03c
출처 메모uspto-grants-2014_07