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HRID 963853作成日:2026年10月26日

Triethylamine → Tert-butyl 1-(aminoimino-methyl)-piperidin-4-ylmethylcarbamate hemisulfite

https://huagongshe.com/reaction/963853

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
反応物Methanesulfonic acid, aminoimino-HCID 9877361—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 1-(aminoimino-methyl)-piperidin-4-ylmethylcarbamate hemisulfiteHCID 131720709—

反応手順

A solution of 130 g of 1,1-dimethylethyl (4piperidinylmethyl)-carbamate in 1300 ml of DMF is treated with 138 ml of triethylamine and 61.8 g of formamidinesulfonic acid and the mixture is stirred at room temperature overnight. The precipitated material is filtered, suspended in 500 ml of ethanol, again filtered off and dried. There are obtained 65.6 g of tert-butyl 1-(aminoimino-methyl)-piperidin-4-ylmethylcarbamate hemisulfite, MS (ISP): 257.4 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763604
出典データセットuspto-grants-1998_06
ORD IDord-86e6069001dc41e4af4476953984ac18
出典メモuspto-grants-1998_06