HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13074422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 20366878 | HCID 20366878 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13074422 | HCID 13074422 | 76% |
Reaction Steps
To 2-amino-1,3,4,6,7,11b-hexahydro-2H-benzo[a]quinolizine hydrochloride (1.38 g), suspended in a solution of triethylamine (2 ml) in dichloromethane (10 ml) stirred at room temperature was added methane sulphonyl chloride (0.570 g) in dichloromethane (5 ml). After stirring for 18 hours, the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.06 g) as an oil, which was converted in ethanolic hydrogen chloride to the hydrochloride (0.395 g) m.p. 244.8° C. C14H20N2O2S.HCl requires C, 53.06; H, 6.68; N, 8.84%. Found: C, 53.07; H, 6.77; N, 8.64%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04076820 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-e64f90f0251b43ceabc13b4042bd4cae |
| Source note | uspto-grants-1978_02 |