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HRID 1585198作成日:2026年10月26日

Diphenyl carbonate → Methyl 4-iodo-2-(3-(4-methoxy-6-methyl-1,3,5-triazine-2-yl)ureidosulfonyl)benzoate

https://huagongshe.com/reaction/1585198

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenyl carbonateHCID 7597—
反応物2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
反応物2-(Aminosulfonyl)-4-iodobenzoic acid methyl esterHCID 10947822—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylacetamideHCID 31374—
生成物Methyl 4-iodo-2-(3-(4-methoxy-6-methyl-1,3,5-triazine-2-yl)ureidosulfonyl)benzoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05936085
出典データセットuspto-grants-1999_08
ORD IDord-03ba43a6334546a5a202ae429f3f7516
出典メモuspto-grants-1999_08