HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358233Generated: October 31, 2026
2-(2-Methoxy-5-morpholin-4-yl-phenylamino)-2-thioxo-acetamide → 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid amide
https://huagongshe.com/reaction/1358233
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(2-Methoxy-5-morpholin-4-yl-phenylamino)-2-thioxo-acetamide | HCID 11254914 | — |
| Catalyst | HCID 178511488 | HCID 178511488 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid amide | HCID 10149480 | — |
Reaction Steps
A suspension of 220 mg (0.75 mmol) 2-(2-methoxy-5-morpholin-4-yl-phenylamino)-2-thioxo-acetamide in 2.88 ml 1N aqueous sodiumhydroxde was added to a solution of 813 mg (2.47 mmol) potassium ferricyanide in 2 ml water. The mixture was stirred at 50° C. for 30 minutes and then at room temperature overnight. The precipitate was separated by filtration, dissolved in dichloromethane and purified by column chromatography on silicagel with ethyl acetate/hexane 1/1. 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid amide, 32 mg (15%), was obtained as yellow crystals with mp.: 228-230° C., MS m/e (%): 294 (M+H+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06596718B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-ed6cafa0947f4a07b092289bf97913bd |
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| Source note | uspto-grants-2003_07 |
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