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HRID 61947作成日:2026年10月26日

Methylamine → Chlorantraniliprole

https://huagongshe.com/reaction/61947

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物2-(3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl)-6-chloro-8-methyl-4H-benzo[d][1,3]oxazin-4-oneHCID 10253307—
溶媒TetrahydrofuranHCID 8028—
生成物ChlorantraniliproleHCID 11271640—

反応条件

温度60 °C

反応手順

To a solution of 2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-chloro-8-methyl-4H-3,1-benzoxazin-4-one (i.e. the benzoxazinone product of Example 5, Step E) (0.20 g, 0.44 mmol) in tetrahydrofuran was added methylamine (2.0 M solution in THF, 0.514 mL, 1.02 mmol), and the reaction mixture was heated to 60° C. for 90 minutes and then cooled to room temperature. The tetrahydrofuran solvent was evaporated under reduced pressure, and the residual solid was triturated with ether, filtered, and dried to afford the title compound, a compound of the present invention, as a solid (40 mg), m.p. 162-164° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09445593B1
出典データセットuspto-grants-2016_09
ORD IDord-2e9e670fe83f48e28754e52734b7a773
出典メモuspto-grants-2016_09