HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808011Generated: October 27, 2026
Magnesium monoperoxyphthalic acid → HCID 178499278, compound
https://huagongshe.com/reaction/1808011
Participants
| Role | Name | HCID | Charge |
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| Reactant | Magnesium monoperoxyphthalic acid | HCID 9815656 | — |
| Reactant | HCID 178499277 | HCID 178499277 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178499278 | HCID 178499278 | 105.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357718B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ff42043f41d24f448abfd5b012cd77c5 |
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| Source note | uspto-grants-2013_01 |
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