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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanethiol | HCID 878 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Thiomorpholine | HCID 67164 | — |
| 反応物 | 1,3-DI-Boc-2-methylisothiourea | HCID 546603 | — |
| 触媒 | Mercurous Chloride | HCID 24182 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | (tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829011B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-ecb393ba31374a78a579de07f0e712fd |
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| 出典メモ | uspto-grants-2014_09 |
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