HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217185Generated: October 30, 2026
Methanesulfonyl chloride → 4-(2-Chloro-2-oxazolo[4,5-c]pyridin-2-ylethyl)piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/217185
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(2-Hydroxy-2-oxazolo[4,5-c]pyridin-2-ylethyl)piperidine-1-carboxylic acid tert-butyl ester | HCID 57659569 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(2-Chloro-2-oxazolo[4,5-c]pyridin-2-ylethyl)piperidine-1-carboxylic acid tert-butyl ester | HCID 57659558 | — |
Reaction Steps
MsCl (29 μL, 0.38 mmol) was added to a stirred solution of 4-(2-hydroxy-2-oxazolo[4,5-c]pyridin-2-yl-ethyl)piperidine-1-carboxylic acid tert-butyl ester (Preparation 7, 110 mg, 0.32 mmol) in anhydrous pyridine (5 mL) at 0° C. After 1 h, more MsCl (29 μL, 0.38 mmol) was added, then the mixture was stirred at 0° C. for an additional 1 h, before being heated under reflux for 1 h. The reaction was concentrated under reduced pressure, then the residue was purified by flash chromatography (EtOAc-IH, 7:3) to furnish the title compound: RT=3.57 min; m/z (ES+)=310.0 [M+2H-t-Bu]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193359B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-ce22e98802404569ada2cc707e7c3afc |
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| Source note | uspto-grants-2012_06 |
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