Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2-Methylimidazo[1,2-a]pyridine | HCID 136742 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178432162 | HCID 178432162 | 27.4% |
Reaction Steps
To a mixture of 3-mercapto-1H-1,2,4-triazole (1.15 g) and N,N-dimethylformamide (15 ml) was added 60% sodium hydride (450 mg). After foaming was completed, N-chlorosuccinimide in small portions was added to the mixture on an ice bath, and stirred at this temperature for 15 minutes. 2-methylimidazo[1,2-a]pyridine (1.0 g) was then added, and the reaction mixture was heated and stirred at room temperature for 1 hour, and then for 3 hours on an oil bath at 70° C. The reaction solution was concentrated under reduced pressure. The residue was washed twice with diethyl ether, and methanol was added to the residue to remove undissolved materials. The filtrate was concentrated, and then crystals precipitated by the addition of water were collected by filtration, washed with water, followed by diethyl ether, and dried to yield the title compound (480 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238720B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-3b7f962087a64baf933ae68db9e574c6 |
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| Source note | uspto-grants-2007_07 |
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