HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Aminoquinoline → HCID 178512524, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Aminoquinoline | HCID 11359 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Reactant | HCID 178479383 | HCID 178479383 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178512524 | HCID 178512524 | — |
Reaction Steps
A mixture of 200 mg. (0.92 m. mol) 4-guanidinobenzoic acid hydrochloride and 190 mg. (0.93 m. mol) of bis-trimethylsilylacetamide in 20 ml. of dry tetrahydrofuran was heated at reflux until a solution was achieved, and then cooled to room temperature. Thionyl chloride (380 mg., 1.86 m. mol) was added and the reaction mixture allowed to stir for 5 min. 8-Aminoquinoline (670 mg., 4.64 m. mol) was added in 5 ml. of tetrahydrofuran and the mixture allowed to stir for 30 min. Water (0.2 ml) was added to the reaction mixture and the solids filtered and dissolved in 60 ml. of methanol and 120 ml. of chloroform. Addition of diethyl ether precipitated the desired product, 153 mg., m.p. 271°-273° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948891 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-8490cd82cfe04590bf4ecd32392ce5f9 |
| Source note | uspto-grants-1990_08 |