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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694451Generated: October 30, 2026

Water → HCID 178496602, compound

https://huagongshe.com/reaction/1694451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 178499307HCID 178499307—
ReactantHCID 178499308HCID 178499308—
SolventMethanol tetrahydrofuran waterHCID 21892291—
ProductHCID 178496602HCID 178496602—
ProductHCID 178496603HCID 178496603—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-(2,6-difluoro-cyclohex-1-enyl)-3-[(trans-4-methoxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester and 5-(2,3-Difluoro-cyclohex-1-enyl)-3-[(trans-4-methoxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (83 mg, 0.16 mmol) in THF:H2O:MeOH (3:1:2) (2 mL), was added LiOH in water (1N) (0.5 mL, 0.5 mmol). The reaction mixture was stirred at 70° C. for 5 h. The mixture was concentrated under reduced pressure on a rotary evaporator and the residue was treated with a solution of 0.1 N HCl and extracted in EtOAc. The EtOAc layer was dried over Na2SO4. Filtration and removal of the solvent under reduced pressure on a rotary evaporator followed by HPLC purification afforded 5-(2,6-difluoro-cyclohex-1-enyl)-3-[(trans-4-methoxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid (3 mg) and 5-(2,3-difluoro-cyclohex-1-enyl)-3-[(trans-4-methoxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid (3 mg) in overall 8% isolated yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158675B2
Source datasetuspto-grants-2012_04
ORD IDord-196ee27c966049a38ab5d43d8ddc638d
Source noteuspto-grants-2012_04