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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472039Generated: October 29, 2026

Potassium Sodium Tartrate → HCID 58269932, compound

https://huagongshe.com/reaction/472039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 67152479HCID 67152479—
SolventDichloromethaneHCID 6344—
ProductHCID 58269932HCID 58269932—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-[5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-propionic acid ethyl ester (220 mg, 0.47 mmol, prepared by the procedure described in Example 11, Step 5) in DCM (4 mL) at −78° C., DIBAL (1M solution in toluene, 2.35 mL, 2.3 mmol) is added, and the mixture is stirred at −78° C. for 3 h. Reaction is warmed up to room temperature, and a saturated aqueous Rochelle's salt solution (6 mL) is carefully added. Stirring is continued for another 1 hour. The organic layer is separated, and the aqueous phase is extracted with DCM. The combined organic solutions are washed with brine, dried over Na2SO4, and concentrated under reduced pressure. Chromatography of the residue affords 3-[5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-propan-1-ol as a colorless oil. 1H NMR: (CDCl3) 8.97 (s, 1H), 7.49 (s, 1H), 7.48 (d, J=12 Hz, 2H), 7.42 (d, J=10 Hz, 2H), 7.32 (s, 1H), 7.27 (t, J=10 Hz, 1H), 7.15 (d, 12 Hz, 2H), 3.76 (t, J=6 Hz, 2H), 3.01 (m, 1H), 2.89 (t, J=6 Hz, 2H), 2.35 (m, 4H), 2.01 (m, 2H), 1.33 (d, J=10 Hz, 6H), 1.073 (t, J=10 Hz, 6H); LCMS m/z 427.32 (2.32 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633193B2
Source datasetuspto-grants-2014_01
ORD IDord-5c64ef5e4ec641f7af8dd150c4bea39c
Source noteuspto-grants-2014_01