HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 178491252, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-Chloroveratraldehyde | HCID 79445 | — |
| Reactant | HCID 178513140 | HCID 178513140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178491252 | HCID 178491252 | — |
Reaction Steps
536 mg (5 mmol) benzylamine and 1.17 g (5 mmol) S′-methylthiosemicarbazide hydroiodide was mixed in 10 ml of ethanol. The reaction mixture was refluxed for 5 minutes after which it was cooled down to room temperature and the residue filtered off. The crude product of N-amino-N′-benzylguanidine was reacted with 1.0 g (5 mmol) 2-chloro-3,4-dimethoxybenzaldehyde under reflux for 5 h, after which the solvent was removed under vacuum to give a white solid. The product was obtained by recrystallisation from methanol. Yield of title compound 1, was 1.65 g (77%). M.p. 0.223–225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153881B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-e3ed2de675fe4f90a8bd5a9256dc2f41 |
| Source note | uspto-grants-2006_12 |