HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348556Generated: October 29, 2026
N,N-Dimethylaniline → N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide
https://huagongshe.com/reaction/348556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 2,4-Dibromo-6-methylpyridin-3-amine | HCID 10084238 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide | HCID 10430271 | 85.3% |
Reaction Steps
3-Amino-2,4-dibromo-6-methylpyridine (1.16 g, 4.38 mmol) was dissolved in methylene chloride (10 mL). N,N-dimethylaniline (0.77 g, 6.35 mmol) was added to the solution and then a solution of bromoacetyl bromide (1.03 g, 5.12 mmol) in dichloromethane (2 mL) was added dropwise thereto over 5 minutes with stirring and cooling with ice. After completion of addition, the temperature of the mixture was elevated to room temperature and stirred for 12 hours. The resultant mixture was washed sequentially with water, an aqueous saturated sodium hydrogencarbonate solution, and saturated brine. Subsequently, the mixture was dried over sodium sulfate anhydrate and concentrated under reduced pressure. The residue was crystallized from hexane-acetone, to thereby yield 1.44 g of N-[2,4-dibromo-6-methylpyridin-3-yl]-2-bromoacetamide as colorless crystals (yield 85.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176306B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-92f2cd66225a4e7194cb3aa099a32d20 |
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| Source note | uspto-grants-2007_02 |
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