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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050592Generated: October 31, 2026

Ethanol → Sodium (3R,5S,E)-7-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3,5-dihydroxy-6-heptenoate

https://huagongshe.com/reaction/2050592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
Reactant7-[4,5-Bis-(4-fluoro-phenyl)-2-isopropyl-imidazol-1-yl]-3,5-dihydroxy-hept-6-enoic acidHCID 14849847—
SolventWaterHCID 962—
ProductSodium (3R,5S,E)-7-[4,5-bis(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3,5-dihydroxy-6-heptenoateHCID 23721969104.5%

Reaction Steps

A suspension of (3R,5S,E)-7-[4,5-bis-(4-fluorophenyl)-2-(1-methylethyl)-1H-imidazol-1-yl]-3,5-dihydroxy-6-heptenoic acid (200 mg) in sodium hydrogen carbonate (36.8 mg) and water (80 ml) was stirred at room temperature. After 19 h ethanol (20 ml) was added and the resulting clear solution stirred at room temperature. After 15 min the mixture was evaporated to dryness, the residue was dissolved in water (50 ml), filtered and then freeze dried to give the title compound (219 mg) as a white fluffy solid, [α]D +22.6° (C 0.53, H2O), δ(D2O) 1.20-1.55, 1.55-1.78 (m, 2H, CH(OH)CH2CH(OH)), 1.33 (d, J 7 Hz, 6H, CH(CH3)2), 2.26 (d, J 7 Hz, 2H, CH2CO2Na), 3.28 (septet, J 7 Hz, 1H, --CH(CH3)2, 3.67 (m, 1H, =CHCH(OH)CH2CH(OH)). 4.35 (m, 1H, CH=CHCH(OH)), 5.49 (dd, J 14 Hz and 7 Hz, 1H, NCH=CH), 6.72 (d, J 14 Hz, 1H, NCH=CH), 6.97 (t, 9 Hz, 2H, C-3 and C-5 protons of 4-fluorophenyl), 6.90-7.40 (m, 6H, aromatics).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013749
Source datasetuspto-grants-1991_05
ORD IDord-fa110642dfe64d67b3efed50cb47cfb2
Source noteuspto-grants-1991_05