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HRID 237123作成日:2026年10月26日

Trifluoroacetic acid → Ethyl 6-ethyl-3,4-dihydro-5-hydroxy-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATE

https://huagongshe.com/reaction/237123

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Ethyl 5-amino-6-ethyl-3,4-dihydro-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATEHCID 12516925—
反応物Potassium trifluoroacetateHCID 23662811—
生成物Ethyl 6-ethyl-3,4-dihydro-5-hydroxy-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATEHCID 23330393—

反応条件

温度25 °C

反応手順

The diazonium fluoborate salt is prepared as in Procedure 63 from the amino compound produced in Procedure 51 yielding 0.03 mole of the required diazonium fluoborate. The latter is added in one portion to a solution of 0.03 mole of potassium trifluoroacetate in 13 ml. of trifluoroacetic acid at 0° C. The mixture is stirred at 25° C. for one hour and then refluxed overnight. The trifluoroacetic acid is evaporated in vacuo to give a residue which is triturated with water and filtered to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04159377
出典データセットuspto-grants-1979_06
ORD IDord-b5eceba6e9d445f4bc3d61216a917bed
出典メモuspto-grants-1979_06