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HRID 72804作成日:2026年10月25日

Methanethiol → (tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/72804

反応式

関与物質

役割名称HCID仕込み量
反応物MethanethiolHCID 878—
反応物TriethylamineHCID 8471—
反応物ThiomorpholineHCID 67164—
反応物1,3-DI-Boc-2-methylisothioureaHCID 546603—
触媒Mercurous ChlorideHCID 24182—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物(tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl esterHCID 67369775—

反応手順

A solution of [[[(1,1-dimethylethoxy)carbonyl]amino]-(methylthio)methylene]-carbamic acid, 1,1-dimethylethyl ester [CAS 107819-90-9] (21 g, 0.0723 mol) in DMF (450 mL) was treated sequentially with thiomorpholine (7 mL, 0.0723 mol), mercury chloride (19.6 g, 0.0723 mol), and Et3N (30 mL, 0.22 mol) and the reaction mixture was stirred for 18 h. The mixture was diluted with EtOAc and filtered through a pad of diatomaceous earth. The filtrate was concentrated, diluted with water and EtOAc and filtered again through a pad of diatomaceous earth. The filtrate aqueous layer was separated and extracted with EtOAc (2×). The combined organic layers were washed with water, then satd. aq. NaCl, dried, and concentrated. The solid was triturated with 20% Et2O/40-60° C. petrol. The solid was filtered off and was washed with 20% Et2O/40-60° C. petrol followed by 40-60° C. petrol. The solid was dried under vacuum to give 21.2 g (85%) as a white solid. Note: The reaction was performed with a trap for gaseous loss of methanethiol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829011B2
出典データセットuspto-grants-2014_09
ORD IDord-ecb393ba31374a78a579de07f0e712fd
出典メモuspto-grants-2014_09