HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512570Generated: November 1, 2026
Benzo(d)thiazol-2-amine → HCID 60148073, compound
https://huagongshe.com/reaction/512570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 68279388 | HCID 68279388 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 60148073 | HCID 60148073 | 799.1% |
Reaction Steps
To a solution of 2-aminobenzothiazole (359.37 ma, 1.0 mmol) in dichloromethane (20 mL) was added 1-Ethyl-3-(3-Dimethylaminopropyl)carbodiimide (EDC) (191 mg, 1.0 mmol) and 1-hydroxy-1,2,3-benzotriazole (HOBt) (13.5 ma, 0.1 mmol). Then added 2-{5-[1-acetyl-3-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-5-pyrazolyl]-2-methoxyphenoxy}acetic acid (3) (458 mg, 0.1 mmol) and the reaction mixture was stirred at a temperature of 25° C. for 24 h and the reaction was monitored by TLC. Then to this water is added and extracted with dichloromethane. The solvent was evaporated under vacuum to afford the crude product. This was further purified by column chromatography using ethyl acetate and hexane as solvent system to obtain the pure product (10a) (472 mg, 80% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102638B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-0843c3fa4fe745bdb5ca03379d959243 |
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| Source note | uspto-grants-2015_08 |
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