HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715227Generated: October 26, 2026
Bromine → N-[5-(bromoacetyl)-4-methyl-1,3-thiazol-2-yl]acetamide, hydrobromide salt
https://huagongshe.com/reaction/1715227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-(5-acetyl-4-methyl-1,3-thiazol-2-yl)acetamide | HCID 830648 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[5-(bromoacetyl)-4-methyl-1,3-thiazol-2-yl]acetamide, hydrobromide salt | HCID 87942046 | 60% |
Reaction Steps
A solution of Br2 (3.35 ml, 65.6 mmol) in 75 ml dioxane is added dropwise to a solution of N-(5-acetyl-4-methyl-1,3-thiazol-2-yl)acetamide (P6), obtained in Step I as described above, (10.40 g, 52.5 mmol) in 200 ml dioxane. The resulting mixture is heated at 50° C. for 19 hours. The solution turns from dark red to beige and remains a heterogeneous mixture. By analytical HPLC, only 2.8% of starting material is detected. The suspension is filtered, washed with a 1:2 EtOAc/hexanes mixture (50 ml) and air dried for 15 min, to give Intermediate 1 as a beige solid (11.2 g, 60%). It is used in bis-thiazol synthesis as HBr salt or as parent, after 5 min treatment with Amberlyst A21 in DCM/MeOH mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799814B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-e4a20fd958ac43b19eea5d4ea87e7ca1 |
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| Source note | uspto-grants-2010_09 |
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