HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839640Generated: October 30, 2026
Methyl iodide → 2-[methyl-N-(methoxycarbonyl)amino]-6-(phenylthio)imidazo[1,2-a]pyridine
https://huagongshe.com/reaction/839640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl [6-(phenylsulfanyl)imidazo[1,2-a]pyridin-2-yl]carbamate | HCID 12414300 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-[methyl-N-(methoxycarbonyl)amino]-6-(phenylthio)imidazo[1,2-a]pyridine | HCID 54049456 | — |
Reaction Steps
A suspension of 1.0 g. (0.0033 moles) of 2-(methoxycarbonylamino)-6-(phenylthio) imidazo [1,2-a] pyridine in 35 ml. of tetrahydrofuran under a argon atmosphere is treated dropwise with 1.35 ml. of a 2.45 molar solution of butyllithium in hexane at -20° C. The resultant solution is stirred for 5 minutes and 0.469 g. (0.0033 moles) of methyliodide is added. The reaction mixture is allowed to warm to room temperature and stirred for 30 minutes. The solution is diluted with ice water and the solids are collected by filtration, washed with water and dried. The solid materials is chromatographed on silica gel and eluted with 1:99 methanol in methylene chloride affording 2-[methyl-N-(methoxycarbonyl)amino]-6-(phenylthio) imidazo [1,2-a] pyridine m.p. 147°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04096264 |
|---|
| Source dataset | uspto-grants-1978_06 |
|---|
| ORD ID | ord-cd4a64b056074811b63300e1b3b02414 |
|---|
| Source note | uspto-grants-1978_06 |
|---|