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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978064Generated: October 31, 2026

Methanesulfonic Acid → HCID 9955564, compound

https://huagongshe.com/reaction/1978064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 86756723HCID 86756723—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 9955564HCID 9955564102.7%

Reaction Steps

A solution of 0.246 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-(methanesulphonyl)-4-methylvalerohydrazide in a mixture of 10 ml of methanol and 2 ml of dichloromethane was treated with 0.006 ml of methanesulphonic acid. The mixture was stirred for 3 hours at room temperature and then the solvent was evaporated. The residue was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over anhydrous magnesium sulphate and the solvent evaporated. The residue was triturated with hexane to give 0.119 g of (E)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2′-isobutyl-2′-(methanesulphonyl)-4-methylvalerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235787B1
Source datasetuspto-grants-2001_05
ORD IDord-3ed720023d49433e976eca424d5769bf
Source noteuspto-grants-2001_05