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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747257생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/747257

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물2,1,3-Benzothiadiazole-4-carboxylic acidHCID 2795202—
용매BenzeneHCID 241—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amideHCID 5974956490%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07396849B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-230e8d73e781496aaa1a8724d53153d1
출처 메모uspto-grants-2008_07