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HRID 1174665作成日:2026年10月27日

Triethylamine → Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide

https://huagongshe.com/reaction/1174665

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物2,1,3-Benzothiadiazole-4-carboxylic acidHCID 2795202—
溶媒BenzeneHCID 241—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amideHCID 5974956490%

反応手順

A suspension of benzo[1,2,5]thiadiazole-4-carboxylic acid (Intermediate L1) (1.8 g, 9.99 mmol) (commercially available from Maybridge) in benzene (100 mL) was treated with oxalyl chloride (5.1 mL of a 2 M CH2Cl2 solution) and DMF (catalytic amount) at rt for 1 h. The solvent was removed under vacuum and re-suspended in benzene. The mixture was decanted into a flask and concentrated under vacuum. The acid chloride intermediate was dissolved in chloroform (10 mL) and added to a solution of N,O-dimethylhydroxylamine-HCl (1.47 g, 15 mmol) (commercially available from Aldrich) and triethylamine (4 mL, 30 mmol) in chloroform (90 mL) at 0° C. The mixture was stirred at rt for 2 h. The mixture was subjected to a standard aqueous work-up. All solvent was removed under vacuum and the residue was purified by chromatography on silica gel with 50% EtOAc:hexane to give benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide (Intermediate L2) 2 g (90% over two steps).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07838545B2
出典データセットuspto-grants-2010_11
ORD IDord-6f4a22cbe71c4bfbbe0b2ed3996fbcf4
出典メモuspto-grants-2010_11