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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219437생성일: 2026년 10월 25일

Pentamethylbenzene → 2-amino-N-(5-chloro-2-pyridinyl)-3-hydroxybenzamide

https://huagongshe.com/reaction/219437

반응식

참여 물질

역할이름HCID투입량
반응물PentamethylbenzeneHCID 12784—
반응물3-benzyloxy-N-(5-chloro-2-pyridyl)-2-nitrobenzamideHCID 18001135—
용매Trifluoroacetic acidHCID 6422—
생성물2-amino-N-(5-chloro-2-pyridinyl)-3-hydroxybenzamideHCID 1800112789.6%

반응 조건

온도40 °C

반응 단계

To 7.44 g of 3-benzyloxy-N-(5-chloro-2-pyridyl)-2-nitrobenzamide were added 40 ml of trifluoroacetic acid and 3.72 g of pentamethylbenzene and the mixture was stirred at 40° C. for one night. The reaction solution was concentrated in vacuo, a saturated aqueous solution of sodium bicarbonate was added to the resulting residue to such an extent that the residue did not become alkaline and the mixture was extracted with chloroform. The organic layer was extracted with a 1N aqueous solution of sodium hydroxide and the aqueous layer was acidified by adding hydrochloric acid thereto and extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, the solvent was evaporated in vacuo and 200 ml of an ethanolic suspension of Raney nickel was added to the resulting residue. The mixture was stirred a hydrogen atmosphere for 6 hours, N,N-dimethylformamide was added and the insoluble matters were filtered off. The solvent was evaporated in vacuo and water was added to the resulting residue. The resulting precipitate was filtered and dried in vacuo to give 4.58 g of 2-amino-N-(5-chloro-2-pyridyl)-3-hydroxybenzamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE043481E1
출처 데이터셋uspto-grants-2012_06
ORD IDord-a4c669ec6dca4913ae9eb46a8375d9dc
출처 메모uspto-grants-2012_06