HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Pyridyl-ethanesulfonyl-valine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-benzyl-L-valine toluene-p-sulphonate | HCID 11567066 | — |
| Reactant | Pyridine-4-sulfonyl Chloride | HCID 11586382 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Pyridyl-ethanesulfonyl-valine benzyl ester | HCID 70058624 | — |
Reaction Steps
To 1 gm of valine benzyl ester p-toluene-sulfonic acid salt in 40 ml of CH2Cl2 at 0° C. was added 1.12 gm of 4-pyridylsulfonyl chloride (U.S. Pat. No. 431,504 (1982)) and 1.9 ml of triethylamine. After 1 hour, the solution was washed with water and extracted with CH2Cl2 (2×100 ml), dried and concentrated. Silica gel column chromotography provided 4-pyridyl-ethanesulfonyl-valine benzyl ester which was treated with 10% Pd/C in methanol under hydrogen atmosphere to provide the desired product in 85% overall yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05648497 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-c58e0f0973e04885b9308fc986a6b2b4 |
| Source note | uspto-grants-1997_07 |