HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850293Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 58546763, compound
https://huagongshe.com/reaction/1850293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 58546996 | HCID 58546996 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58546763 | HCID 58546763 | 180% |
Reaction Steps
To a mixture of 3-(3-chloro-quinoxalin-2-yl)-azetidine-1-carboxylic acid tert-butyl ester (91) (0.16 g, 0.50 mmol) and piperidine (0.085 g, 1.0 mmol) was added triethylamine (0.10 g, 1.0 mmol) and DMSO (3 mL). The solution was heated to 160° C. in microwave for 2 h. Then the mixture was diluted with water (10 mL) and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water (10 mL) and brine (10 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 50% EtOAc in petroleum ether) to give 3-(3-piperidin-1-yl-quinoxalin-2-yl)-azetidine-1-carboxylic acid tert-butyl ester (92) (0.16 g, 0.90 mmol, 90% yield) as a white solid. ESI-MS (M+1): 369 calc. for C21H28N4O2 368.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957073B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c83532357a5c454c9c98f58f2374edf6 |
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| Source note | uspto-grants-2015_02 |
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