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HRID 439905作成日:2026年10月25日

5-Methyl-2-pyrazinecarboxylic acid → 2-Pyrazinecarboxylic acid, 5-methyl-, methyl ester

https://huagongshe.com/reaction/439905

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methyl-2-pyrazinecarboxylic acidHCID 122831—
反応物4-(2-(5-Methylpyrazine-2-carboxamido)ethyl)benzenesulfonamideHCID 9883549—
溶媒MethanolHCID 887—
生成物2-Pyrazinecarboxylic acid, 5-methyl-, methyl esterHCID 465065—

反応手順

According to the invention there is provided a process for the preparation of N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-methylpyrazine-carboxamide of the formula I: ##STR15## consisting of: i) treating 5-methylpyrazine-2-carboxylic acid of the formula VIII: ##STR16## with methanol under reflux to obtain 5-methylpyrazine-2-carboxylic acid methyl ester of the formula VIII A ##STR17## ii) reacting 5-methylpyrazine-2-carboxylic acid methyl ester of the formula VIII A with 2-phenylethylamine of the formula II: ##STR18## at 100° to 200° C. to obtain 5-methylpyrazine 2-(2-phenylethyl) carboxamide of the formula IX: ##STR19## iii) chlorosulfonating the 5-methylpyrazine-2(2-phenylethyl)carboxamide of the formula IX with chlorosulfonic acid at 0°-45° C. to obtain [N-[2-[4-Chlorosulfonyl)phenyl]ethyl]-5-methylpyrazine carboxamide] of the formula X: ##STR20## iv) and treating the (N-[2-[4-(chlorosulfonyl)phenyl]ethyl]-5-methyl pyrazine-carboxamide] of the formula X with ammonia to obtain N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-methylpyrazine carboxamide of the formula I.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05516906
出典データセットuspto-grants-1996_05
ORD IDord-2edf1d1ea0ff4df987de622771f7d18a
出典メモuspto-grants-1996_05