HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628253Generated: October 29, 2026
Phenethyl bromide → HCID 118159836, compound
https://huagongshe.com/reaction/628253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 136963115 | HCID 136963115 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118159836 | HCID 118159836 | — |
Reaction Steps
To a mixture of 1-methyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridine (10 mg, 0.058 mmol, isolated from Example 2, Step 5 during a preparation wherein the methylation of Step 2 of that Example was incomplete) and K2CO3 (0.024 g, 0.17 mmol) in DMF (0.22 mL) was added 1-(bromoethyl)benzene (12 μL, 0.087 mmol, Acros). The mixture was heated to 45° C. for 3 hours. The mixture was diluted with MeCN and filtered, then the product was isolated by preparative HPLC-MS (Waters XBridge C18, eluting with a gradient of MeCN/H2O containing 0.15% NH4OH) (3.3 mg, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309246B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-5465aca40aaa418bbdbeb2ea3697b0a5 |
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| Source note | uspto-grants-2016_04 |
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