HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303671Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 18187475, compound
https://huagongshe.com/reaction/2303671
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 | 86% |
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-(t-butoxycarbonyl)-4-(1-(RS)-hydroxy-2-(RS)-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 40 S silica cartridge using 2:1 v/v hexanes/ethyl acetate as the eluent afforded 435 mg (85%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06432981B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-beb450785fd84a879bd2d246b9410e64 |
|---|
| Source note | uspto-grants-2002_08 |
|---|