HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58845258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 18452901 | HCID 18452901 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58845258 | HCID 58845258 | 100% |
Reaction Steps
To an ice-cooled solution of ethyl (3S, 4aS, 6R, SaR)6-hydroxy-2-methoxycarbonyl-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline-3-carboxylate (760 mg, 2.66 mmol) in dry dichloromethane (10 mL) under nitrogen, triethylamine (0.60 mL, 4.3 mmol) and methanesulfonyl chloride (0.33 mL, 4.3 mmol) were added. The resulting mixture was stirred overnight at room temperature and a saturated solution of ammonium chloride was added (10 mL). The layers were separated and the aqueous layer extracted with dichloromethane (10 mL×2). The combined organic phases were washed with 1 N hydrochloric acid (10 mL), dried over sodium sulfate and concentrated in vacuo to give the title compound as an oil (0.965 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205313B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-bdfb227d40bf4f77a3ac1d4a203a4609 |
| Source note | uspto-grants-2007_04 |