HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2S)-2-[(4-morpholinylsulfonyl)amino]-3-phenylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Morpholin-4-ylsulfamyl chloride | HCID 13271200 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2S)-2-[(4-morpholinylsulfonyl)amino]-3-phenylpropanoic acid | HCID 10859978 | — |
Reaction Steps
A solution of L-PHE (66 g), NaOH (16 g), and water (120 mL) was treated dropwise with a solution of 4-morpholinylsulfamyl chloride (37 g, prepared according to the methods of R. Wegler and K. Bodenbenner, Anallen der Chemie, 624, 25 (1959) and G. Weiss and G. Schulze, Anallen der Chemie, 729, 40 (1969)) in THF (80 mL). The reaction was stirred for 6 hours at room temperature then concentrated aqueous HCl was added dropwise to bring the solution to pH 2. Product was extracted into EtOAc and this solution was washed with lN HCl, dried over MgSO4 and evaporated. The residue was triturated with ether to give a solid that was recrystallized from water to give morpholinylsulfonyl-PHE. MP 157°-158° C. MS (FAB) 337 (m+Na), 315 (m+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041552 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-546e9386e35a4ba6826c8908953c2186 |
| Source note | uspto-grants-1991_08 |