HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21109929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 21109928 | HCID 21109928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21109929 | HCID 21109929 | — |
Reaction Steps
1.64 ml. (21 mmol) of methanesulphonyl chloride was added dropwise to a solution of 7.91 g (20 mmol) of N-(1,1-dimethylethoxycarbonyl)-N-[(2-aminophenyl)methyl]-1-(phenylmethyl)-4-piperidineamine and 3.0 ml (21 mmol) of triethylamine in 100 ml of tetrahydrofuran and the mixture was then kept for 12 hours at ambient temperature. It was then diluted with 100 ml of EE and extracted twice with 70 ml of saturated sodium hydrogen carbonate solution. The ethyl acetate phase was dried over sodium sulphate and concentrated by evaporation in vacuo. 8.7 g (92% of theoretical) of a colourless substance were obtained, Rf 0.85 (El D), which were used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230001B1 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-2276117a2a99496cbec32e38cdedf1cd |
| Source note | uspto-grants-2007_06 |