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HRID 1476作成日:2026年10月24日

Triethylamine → Isopropyl 3(2-chloro-4-fluoro-5-isothiocyanatophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate

https://huagongshe.com/ja/reaction/1476

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物ThiophosgeneHCID 10040—
反応物isopropyl 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetateHCID 57313385—
溶媒TetrahydrofuranHCID 8028—
生成物Isopropyl 3(2-chloro-4-fluoro-5-isothiocyanatophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetateHCID 11729649—

反応手順

Thiophosgene (0.50 mL, 6.5 mmol) is added over 45 minutes to a solution of isopropyl 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-5-methyl-2,4,6-trioxo-s-triazine-1(2H)-acetate (2.5 g, 6.5 mmol), and triethylamine (1.8 mL, 13.0 mmol) in tetrahydrofuran. The reaction mixture is stirred at room temperature for 4 hours, diluted with tetrahydrofuran, and filtered. The filtrate is concentrated in vacuo to give the title product as an orange oil which is identified by NMR spectral analyses, Using essentially the same procedure, but using the appropriately substituted 3-(5-amino-2-chloro-4-fluorophenyl)tetrahydro-2,4,6-trioxo-s-triazine, the following compounds are obtained:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726126
出典データセットuspto-grants-1998_03
ORD IDord-abde48b4f1894595a808afe5690eeb6d
出典メモuspto-grants-1998_03