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HRID 219437作成日:2026年10月26日

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

https://huagongshe.com/reaction/219437

反応式

関与物質

役割名称HCID仕込み量
反応物PentamethylbenzeneHCID 12784—
反応物3-benzyloxy-N-(5-chloro-2-pyridyl)-2-nitrobenzamideHCID 18001135—
溶媒Trifluoroacetic acidHCID 6422—
生成物2-amino-N-(5-chloro-2-pyridinyl)-3-hydroxybenzamideHCID 1800112789.6%

反応条件

温度40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE043481E1
出典データセットuspto-grants-2012_06
ORD IDord-a4c669ec6dca4913ae9eb46a8375d9dc
出典メモuspto-grants-2012_06