HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243433Generated: November 1, 2026
Pyridine → 4-Nitro-N-(1,3-thiazol-2-yl)benzamide
https://huagongshe.com/reaction/2243433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-Nitro-N-(1,3-thiazol-2-yl)benzamide | HCID 230363 | 96% |
Reaction Steps
2-Aminothiazole (100 mmol) was suspended in 1,2-dichloroethane (200 mL) and pyridine (100 mmol) was added. The mixture was added portion wise to a suspension of 4-nitro benzoic acid chloride (150 mmol) in 1,2-dichloroethane (500 mL) and stirred at 60° C. over night. The reaction mixture was cooled and filtered. The filtrate was washed with 1,2-dichloroethane and dried in vacuo to give 4-nitro-N-thiazol-2-yl-benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674912B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-897392f68707407c831bba52d0a22bb6 |
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| Source note | uspto-grants-2010_03 |
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