HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491847Generated: October 27, 2026
Bromine → 2-Acetylaminomethyl-4-bromoacetylthiazole
https://huagongshe.com/reaction/1491847
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Acetyl-2-(acetylaminomethyl)thiazole | HCID 10012967 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Acetylaminomethyl-4-bromoacetylthiazole | HCID 18953911 | — |
Reaction Steps
Bromine (2.2 g) was added slowly to a solution of 4-acetyl-2-acetylaminomethylthiazole (2.2 g) in acetic acid (20 ml) and water (20 ml), and the mixture was heated at 70° C. for 4 hours. The solvent was removed under reduced pressure to give crude product of 2-acetylaminomethyl-4-bromoacetylthiazole. The above residue was dissolved in ethanol (50 ml). Diaminomethylenethiourea (1.3 g) was added to the solution and the mixture was refluxed for 4 hours. The solvent was removed under reduced pressure. The residue was dissolved in water and then the solution was alkalized with a saturated aqueous potassium carbonate solution. The resulting precipitate was collected by filtration. The filtrate was extracted by ethyl acetate and then the solvent was removed under reduced pressure. The residue and the precipitate were chromatographed on an alumina column eluting with a mixture of chloroform and methanol (10:1). Recrystallization from water afforded 4-(2-acetylaminomethylthiazol-4-yl)-2-(diaminomethyleneamino)thiazole (430 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371097 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-79f44a918d3648a9bc4224d4667726b7 |
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| Source note | uspto-grants-1994_12 |
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