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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808011Generated: October 27, 2026

Magnesium monoperoxyphthalic acid → HCID 178499278, compound

https://huagongshe.com/reaction/1808011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium monoperoxyphthalic acidHCID 9815656—
ReactantHCID 178499277HCID 178499277—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178499278HCID 178499278105.6%

Reaction Steps

To a stirred solution of 3-[(trans-4-methyl-cyclohexanecarbonyl)-(tetrahydro-thiopyran-4-yl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester (57 mg, 0.124 mmol)in EtOH (1.2 mL) from step 2 was added magnesium monoperoxyphthalic acid (29.6 mg, 0.06 mmol) in one portion, stirred for 24 h. Reaction mixture was diluted with water, extracted with EtOAc. The combined organic solution was washed with brine, dried, and concentrated. Purification of the residue on Preparative TLC using 5% MeOH-DCM gave 3-[(trans-4-methyl-cyclohexanecarbonyl)-(1-oxo-tetrahydro-thiopyran-4-yl)-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester (30 mg, 51%). NMR 1H (CDCl3, 400 MHz, For major isomer): 7.66-7.6 (m, 2H), 7.5-7.4 (m, 3H), 7.09 (s, 1H), 4.84-4.76 (t, 1H), 3.85 (s, 3H), 3.4-1.2 (m), 0.772 (d, J=6.6, 3H), 0.74-0.56 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357718B2
Source datasetuspto-grants-2013_01
ORD IDord-ff42043f41d24f448abfd5b012cd77c5
Source noteuspto-grants-2013_01