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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408293Generated: October 30, 2026

Water → (5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione L-tartrate

https://huagongshe.com/reaction/2408293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPioglitazone HydrochlorideHCID 60560—
ReactantL-Tartaric acidHCID 444305—
SolventMethanolHCID 887—
Product(5R)-5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione L-tartrateHCID 86651733—

Reaction Steps

5-{4-[2-(5-ethylpyridin-2-yl)ethoxy]benzyl}-1,3-thiazolidine-2,4-dione hydrochloride (100 mg) in MeOH (2 mL) was stirred for 5 min. using brief sonication to give a clear solution. L-tartaric acid (38 mg, 1 eq) was added followed by dropwise addition of water until a haziness persisted (up to 2 mL used). The reaction was stirred in closed vial for 96 h, the precipitated solid was collected on a filter cup and washed with H2O-MeOH (2:1, 3 ml) and then dried under vacuum (42 mg). (Method 13) 48.30%, Rt 9.62 min.; 51.60%, Rt 14.30 min.; d.e. 3.3%. 1H NMR (400 MHz, DMSO-d6): δ 8.34-8.29 (1H, d, J 1.9), 7.55-7.49 (1 H, dd, J 2.2, 7.9), 7.24-7.20 (1 H, d, J 7.8), 7.12-7.05 (2 H, d, J 8.6), 6.84-6.77 (2 H, d, J 8.6), 4.78-4.71 (1 H, dd, J 4.3, 9.1), 4.30-4.19 (1 H, d, J 4.3), 3.24-3.18 (2 H, d), 3.11-3.03 (2 H, t, J 6.6), 3.00-2.92 (1 H, dd, J 9.2, 14.2), 2.59-2.50 (2 H, q, J 7.6), 1.17-1.09 (3 H, t, J 7.7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815837B2
Source datasetuspto-grants-2014_08
ORD IDord-25e0dc7924084787b3226a5ef4802c16
Source noteuspto-grants-2014_08