HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245577Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 18187475, compound
https://huagongshe.com/reaction/1245577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18187644 | HCID 18187644 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18187475 | HCID 18187475 | — |
Reaction Steps
A solution of oxalyl chloride (0.34 mL, 3.9 mmol) in methylene chloride (12 mL) at −78° C. was treated with DMSO (0.43 mL, 6.0 mmol) and the resulting mixture was stirred cold for 10 min. A solution of 1-(tert-butoxycarbonyl)-4-(1-(R/S)-hydroxy-2-(R/S)-methyl-3-oxopent-1-yl)piperidine (514 mg, 1.7 mmol) (from Step C) was added and the resulting solution was stirred cold for 1 h. N,N-Diisopropylethylamine (2.4 mL, 13.7 mmol) was added and the resulting mixture was warmed to 0° C. The reaction was quenched with 1.0 N HCl (25 mL) and extracted with ether (100 mL). The extract was dried over magnesium sulfate and concentrated. MPLC (Biotage) on a 40S silica cartridge using 2:1 v/v hexanes/ethyl acetate as the eluent afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125887B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-6e42e0700d194d96847a7fa0fb73775d |
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| Source note | uspto-grants-2006_10 |
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