HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073800Generated: November 2, 2026
Triethylamine → 8-(2-Methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/2073800
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyl-6-methoxycarbonylaminobenzyl chloride | HCID 14368480 | — |
| Reactant | 8-Amino-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine | HCID 14499805 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-(2-Methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine | HCID 14499825 | 38.8% |
Reaction Steps
To a solution of 8-amino-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine (8.0 g) and triethylamine (4.8 g) in methanol (80 ml) was added 2-methyl-6-methoxycarbonylaminobenzyl chloride (10.15 g) and the mixture was stirred at room temperature for 17 hours. After methanol was evaporated in vacuo, the resultant residue was dissolved in methylene chloride (100 ml) and the mixture was washed with water and dried over magnesium sulfate. The solvent was evaporated in vacuo. The resultant residue was subjected to column chromatography on silica gel (240 g) and eluted with a mixture of chloroform and ethyl acetate (20:1) to give a crystalline product. The crystals were recrystallized from a mixture of ethyl acetate and n-hexane to give 8-(2-methyl-6-methoxycarbonylaminobenzylamino)-3-(2-propynyl)-2-methylimidazo[1,2-a]pyridine (6.08 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04920129 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-667a7a3e21ed4e049018afdfeeeac1ca |
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| Source note | uspto-grants-1990_04 |
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