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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303671Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 18187475, compound

https://huagongshe.com/reaction/2303671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18187644HCID 18187644—
SolventDichloromethaneHCID 6344—
ProductHCID 18187475HCID 1818747586%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-beb450785fd84a879bd2d246b9410e64
Source noteuspto-grants-2002_08