HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185497Generated: November 3, 2026
Dimethyl Sulfoxide → (2s,4r)-n-Tert-butoxycarbonyl-4-(n-tert-butoxycarbonylglycylamino)-2-pyrrolidinecarboxaldehyde
https://huagongshe.com/reaction/2185497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2s,4r)-4-(n-Tert-butoxycarbonylglycylamino)-2-hydroxymethyl-n-tert-butoxycarbonylpyrrolidine | HCID 70172939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2s,4r)-n-Tert-butoxycarbonyl-4-(n-tert-butoxycarbonylglycylamino)-2-pyrrolidinecarboxaldehyde | HCID 73947491 | 97.9% |
Reaction Steps
The following reaction was carried under argon. Dimethyl sulfoxide (288 μL) was added to a stirred solution of oxalyl chloride (177 mL) in dichloromethane (3 mL) at −78° C. After stirring at the same temperature for 15 min, a solution of (2S,4R)-N-tert-butoxycarbonyl-4-(N-tert-butoxycarbonylglycylamino)-2-hydroxymethylpyrrolidine (151 mg) in dichloromethane (3 mL) was added. The mixture was stirred at −78° C. for 2 hr, and triethylamine (848 μL) was added to the reaction mixture. The mixture was stirred at 0° C. for 1 hr, quenched with saturated ammonium chloride, and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform then chloroform:methanol=99:1 to 97:3, v/v) to give the titled compound (147 mg) as a colorless foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06399629B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-03fc29335e094994a8fa838f145795ca |
|---|
| Source note | uspto-grants-2002_06 |
|---|