HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363269Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 71143526, compound
https://huagongshe.com/reaction/2363269
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 minutes. 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 hour, and then triethylamine (7.04 mL, 50.5 mmol) was added. The mixture was stirred at −78° C. for an additional 1.5 hour. 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 reaction without further purification. LCMS (M+H)+: m/z 233.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691807B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2d6092df0b954e9ba4dc340a0b85bccb |
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| Source note | uspto-grants-2014_04 |
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