HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-3-Aminomethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl (3S)-3-(azidomethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate | HCID 131733307 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-3-Aminomethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester | HCID 57364940 | — |
Reaction Steps
To a solution of 20.9 g (64.5 mmol) of the azido compound obtained in Step B in 650 mL of THF, there are successively added 25.5 g (97.2 mmol) of triphenylphosphine and 157 mL of water. The batch is refluxed for 2 hours 30 minutes. The reaction mixture is then concentrated to dryness and the residue oil is then taken up in isopropyl ether. A white precipitate appears; it is filtered off and washed with isopropyl ether. The filtrate is then concentrated to dryness and then purified by chromatography over silica gel using dichloromethane and methanol as eluants. The title product is obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108983B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-32ac413e4b954849b452c1de0a6b6f40 |
| Source note | uspto-grants-2015_08 |