HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178512526, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Bistrimethylsilylacetamid | HCID 11708267 | — |
| Reactant | HCID 14819960 | HCID 14819960 | — |
| Reactant | HCID 178512548 | HCID 178512548 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178512526 | HCID 178512526 | — |
Reaction Steps
A mixture of 970 mg. (4.48 m. mol) of 4-guanidinobenzoic acid and 910 mg. (4.48 m. mol) of bis-trimethylsilylacetamide in dry tetrahydrofuran was heated to reflux for five minutes. After cooling the resulting solution of thionylchloride, 1.07 g. (8.95 m. mol) was added, followed after 20 minutes by the addition of 1.5 g. (8.95 m. mol) of 2-amino-5-chloroimidazole and 1.81 g. (17.9 m. mol) of triethyl amine in 10 ml. of tetrahydrofuran. After 16 hours at room temperature 0.40 ml. of water was added and the solids filtered, washed with chloroform and recrystallized from methanol-chloroform-diethyl ether, 435 mg., m.p. 263°-265° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948901 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-9eba385bfa8049198494ef2d702ac629 |
| Source note | uspto-grants-1990_08 |