HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51868Generated: October 26, 2026
Dimethylformamide → 4-methoxy-N7,N7-dimethyl-benzothiazole-2,7-diamine
https://huagongshe.com/reaction/51868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxy-1,3-benzothiazole-2,7-diamine | HCID 22736977 | — |
| Product | 4-methoxy-N7,N7-dimethyl-benzothiazole-2,7-diamine | HCID 22737002 | 26% |
Reaction Steps
To a stirred solution of 2.00 g (1.02 mmol) 4-methoxy-benzothiazole-2,7-diamine in 30 ml DMF at room temperature was added 4.25 g (3.07 mmol) potassium carbonate and the mixture heated to 50° C. A solution of 0.64 ml (1.02 mmol) iodomethane in 10 ml DMF was then added dropwise over 3 h and stirring continued for a further 1 h at 50° C. The mixture was then filtered and the filtrate concentrated in vacuo. Flash chromatography (20/1 dichloromethane/methanol) afforded 600 mg (26%) 4-methoxy-N7,N7-dimethyl-benzothiazole-2,7-diamine as a yellow solid, ES-MS m/e (%): 224 (M+H+, 100); 540 mg (25%) 4-methoxy-N7-methyl-benzothiazole-2,7-diamine as a yellow solid, ES-MS m/e (%): 210 (M+H+, 100) and 340 mg (17%) recovered starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713499B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-3e7177a036404a6987b0414536212ffc |
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| Source note | uspto-grants-2004_03 |
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