関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diphenyl carbonate | HCID 7597 | — |
| 反応物 | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| 反応物 | 2-(Aminosulfonyl)-4-iodobenzoic acid methyl ester | HCID 10947822 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | Methyl 4-iodo-2-(3-(4-methoxy-6-methyl-1,3,5-triazine-2-yl)ureidosulfonyl)benzoate | HCID 11027582 | — |
反応手順
2.59 g of potassium tert-butylate was added to a suspension of 2.85 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 40 ml of dimethylacetamide (DMA) at room temperature to form a first mixture. A solution of 4.94 g of diphenyl carbonate in 20 ml of DMA was then added dropwise to the first mixture at about 5° C. to form a second mixture. The second mixture was subsequently added dropwise to a solution of 5.00 g of methyl 2-aminosulfonyl-4-iodobenzoate (92.5% pure) in 15 ml of DMA at about 5° C., to form a third mixture. When the reaction ended, the third mixture was filtered over kieselguhr (®Celite). The filtrate was introduced into a solution of 200 ml of ice-water and 10 ml of concentrated hydrochloric acid, whereby the crude urea product separated out. The crude product which separated out was then purified by stirring with methanol and diisopropyl ether and dried. The yield was 4.50 g (66% of theory).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05936085 |
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| 出典データセット | uspto-grants-1999_08 |
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| ORD ID | ord-03ba43a6334546a5a202ae429f3f7516 |
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| 出典メモ | uspto-grants-1999_08 |
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