HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747257Erstellt: 25. Oktober 2026
Triethylamine → Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide
https://huagongshe.com/reaction/747257
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Edukt | 2,1,3-Benzothiadiazole-4-carboxylic acid | HCID 2795202 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Benzo[1,2,5]thiadiazole-4-carboxylic acid methoxy-methyl-amide | HCID 59749564 | 90% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07396849B2 |
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| Quelldatensatz | uspto-grants-2008_07 |
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| ORD ID | ord-230e8d73e781496aaa1a8724d53153d1 |
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| Quellennotiz | uspto-grants-2008_07 |
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