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HRID 2071308作成日:2026年10月26日

Sulfuric Acid → HCID 178513793、化合物

https://huagongshe.com/reaction/2071308

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物2-Chloro-5-phenylpyrazineHCID 1236664—
反応物2-Chloro-6-phenylpyrazineHCID 5216092—
反応物alpha-Methyl-6-phenylpyrazineacetic acidHCID 21413159—
反応物Ethyl alpha-methyl-5-phenylpyrazineacetateHCID 21413165—
反応物Ethyl alpha-methyl-6-phenylpyrazineacetateHCID 21413174—
反応物alpha-Methyl-6-phenylpyrazineacetamideHCID 21413182—
反応物Diethyl alpha-methyl-6-phenylpyrazinylmalonateHCID 21413214—
反応物Diethyl alpha-methyl-5-phenylpyrazinylmalonateHCID 21413242—
反応物HCID 178516747HCID 178516747—
反応物HCID 178516765HCID 178516765—
生成物HCID 178513793HCID 178513793—

反応手順

3-Hydroxy-5-phenylpyrazine-2-carboxamide is prepared by the method of Dick, Wood and Logan, J. Chem. Soc., 2131 (1956). The carboxamide is converted to 6-phenylpyrazinol by the method of Jezo and Luzak, Chem. Zvest., 22, 190 (1968), using 80 percent sulfuric acid at 180° C. Using the procedure of Example III and replacing 5-phenylpyrazinol with an equivalent amount of 6-phenylpyrazinol, the product obtained is 2-chloro-6-phenylpyrazine. Using the procedure of Example V and replacing 2-chloro-5-phenylpyrazine with an equivalent amount of 2-chloro-6-phenylpyrazine, the product obtained is diethyl α-methyl-6-phenylpyrazinylmalonate. Using the procedure of Example VI and replacing diethyl α-methyl-5-phenylpyrazinylmalonate with an equivalent amount of diethyl α-methyl-6-phenylpyrazinylmalonate, the product obtained is ethyl α-methyl-6-phenylpyrazineacetate. Using the procedure of Example IX and replacing ethyl α-methyl-5-phenylpyrazineacetate with an equivalent amount of ethyl α-methyl-6-phenylpyrazineacetate, the product obtained is α-methyl-6-phenylpyrazineacetic acid. Using the procedure of Example XI and replacing ethyl α-methyl-5 -phenylpyrazineacetate with an equivalent amount of ethyl α-methyl-6-phenylpyrazineacetate, the product obtained is α-methyl-6-phenylpyrazineacetamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04046763
出典データセットuspto-grants-1977_09
ORD IDord-c596032506e84caf8b313540b0e2a135
出典メモuspto-grants-1977_09