HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-N,N-dimethyl-1-propanamine → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | 5-(3,4-Dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one | HCID 15340822 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 3-Dimethylaminopropyl-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one | HCID 9929063 | — |
Reaction Steps
0.6 g of potassium tert-butylate is added to a solution of 1.5 g of 5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one [obtainable by reacting 1-(3,4-dimethoxyphenyl)-2-bromobutan-1-one with methyl hydrazinethioformate] in 30 ml of dimethylformamide (DMF), and the mixture is stirred for 30 minutes. A solution of 3-chloropropyldimethylamine in toluene is then added and the mixture is boiled for three hours. The solvent is removed in vacuo, and the mixture is worked up as usual to give 3-dimethylaminopropyl-5-(3,4-dimethoxyphenyl)-6-ethyl-3,6-dihydro-1,3,4-thiadiazin-2-one, m.p. 175° (hydrochloride).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434149 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-7b90bf00e9e242f18fdb30b4c0d60884 |
| Source note | uspto-grants-1995_07 |