HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049134Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 71143526, compound
https://huagongshe.com/reaction/1049134
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(3-Hydroxy-1-azetidinyl)-N-(1-methylethyl)benzamide | HCID 71143534 | — |
| Product | HCID 71143526 | HCID 71143526 | 77.4% |
Reaction Steps
To a cooled (−78° C.) solution of oxalyl chloride (1.05 mL, 12.4 mmol) in dichloromethylene (20 mL) was added dropwise dimethyl sulfoxide (1.71 mL, 24.1 mmol). The mixture was stirred at −78° C. for 10 min. Then a suspension of 4-(3-hydroxyazetidin-1-yl)-N-isopropylbenzamide (1.72 g, 7.34 mmol) in dichloromethylene (20 mL) was added. The mixture was stirred at −78° C. for 1 h, and then triethylamine (7.04 mL, 50.5 mmol) was added. The mixture was stirred at −78° C. for an additional 1.5 h. The mixture was washed with aq. NaHCO3 and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The precipitates were washed with ether and collected by filtration to afford the desired product (1.32 g, 77%) which was directly used in the next step without further purification. LCMS cacld. for C13H17N2O2 (M+1)+: m/z=233.1. Found: 233.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382231B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-08838eb3509b47c79edf1c364a31fda8 |
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| Source note | uspto-grants-2016_07 |
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