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HRID 2066948作成日:2026年10月25日

Diethyl 5-amino-3-methylthiophene-2,4-dicarboxylate → 2-(2-Benzyloxycarbonylaminoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylic acid

https://huagongshe.com/reaction/2066948

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl 5-amino-3-methylthiophene-2,4-dicarboxylateHCID 78537—
反応物benzyl N-(2-cyanoethyl)carbamateHCID 262127—
生成物2-(2-Benzyloxycarbonylaminoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylic acidHCID 69077067—

反応手順

Using diethyl 5-amino-3-methylthiophene-2,4-dicarboxylate and benzyl N-(2-cyanoethyl)carbamate, the ring-closing reaction was carried out similarly to Production Example 1. Successively the hydrolysis was carried out similarly to Example 1, to provide 2-(2-benzyloxycarbonylaminoethyl)-5-methyl-4-oxo-3,4-dihydrothieno[2,3-d]pyrimidine-6-carboxylic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08293754B2
出典データセットuspto-grants-2012_10
ORD IDord-688097459afe475a94f7ce25b7f965aa
出典メモuspto-grants-2012_10