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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038083Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 86614441, compound

https://huagongshe.com/reaction/1038083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 86614440HCID 86614440—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86614441HCID 8661444166%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Added DMSO (200 mg, 2.56 mmol) to a solution of oxalyl chloride (180 mg, 1.40 mmol) in MeCl2 (10 ml) at −78° C., then stirred at −78° C. for 1 hour. Added 3-(1-Hydroxy-ethyl)-1-{2-[2-methyl-4-(5-pyrimidin-2-yl-pyridin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-pyrrolidine-3-carboxylic acid [3-(4-fluoro-phenyl)-1Trityl-indazol-5-yl]-amide (9N) in MeCl2 (5 ml) at −78° C. then stirred at −78° C. for 2 hours. Triethylamine (200 mg, 1.96 mmol) was added, the solution allowed warm to room temperature then stirred overnight. Added water (50 ml) and MeCl2 (150 ml). The organic layer was separated, dried over MgSO4, filtered and solvent evaporated yielding 10N as a solid (600 mg, 66%) ESMS (MH, 904)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546404B2
Source datasetuspto-grants-2013_10
ORD IDord-54f12418fb1346a4bcc67553895e35e9
Source noteuspto-grants-2013_10