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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451865Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 59201564, compound

https://huagongshe.com/reaction/451865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantNitrogenHCID 947—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59201451HCID 59201451—
SolventDichloromethaneHCID 6344—
ProductHCID 59201564HCID 5920156445.8%

Reaction Conditions

Temperature-65 °C

Reaction Steps

A solution of DMSO (0.82 g, 10.47 mmol) in 10 mL of dry CH2Cl2, under protection of N2, was cooled to −78° C., followed by the slow, dropwise addition of oxalyl chloride (0.664 g, 5.23 mmol). After addition the mixture was stirred 2 hr at −65° C., then the solution of (S)-tert-butyl 1-(4-hydroxycyclohexyl)-3-(N-methyl-N-(benzyloxycarbonyl)amino)propan-2-ylcarbamate (1.1 g, 2.62 mmol) was added dropwise. After addition, the mixture was stirred 3 hr at −30° C. The reaction was quenched with Et3N (4 mL) and stirred 10 min, then saturated NaHCO3 (10 mL) was added. The aqueous layer was extracted 3 times with CH2Cl2 (3×20 mL). The CH2Cl2 layer was washed with 10% citric acid solution (20 mL), followed by saturated NaHCO3, brine, then dried over Na2SO4. After filtration, solvent removal gave crude product (1 g), which was purified by preparative TLC to give (S)-tert-butyl 1-(N-methyl-N-(benzyloxycarbonyl)amino)-3-(4-oxocyclohexyl)propan-2-ylcarbamate (500 mg, 1.2 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-38ae103994514255ba8e825e7dc70508
Source noteuspto-grants-2013_07