HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14839448, compound → Imidazo(4,5-b)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14839448 | HCID 14839448 | — |
| Reactant | HCID 178527819 | HCID 178527819 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imidazo(4,5-b)pyridine | HCID 67504 | — |
Reaction Steps
2-Mercaptoimidazo[4,5-b]pyridine and 2-(N-cylopentylamino)benzyl chloride hydrochloride were reacted in an aqueous ethanol solution to obtain 2-[2-(N-cyclopentylamino)benzylthio[-imidazo[4,5-b]pyridine in the same manner as in Example 9-(2). The obtained 2-[2-(N-cyclopentylamino)benzylthio]imidazo[4,5-b]pyridine was oxidized by m-chloroperbenzoic acid in chloroform in the same manner in Example 9-(3) to give 2-[2-(N-cyclopentylamino)benzylsulfinyl]imidazo[4,5-b]pyridine as a pale yellow crystalline product. m.p.: 134° C. (decompn.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933458 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-71a1d152df244e14af615d7a91daf7e1 |
| Source note | uspto-grants-1990_06 |