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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177419Generated: November 1, 2026

Ammonium Hydroxide → HCID 59174896, compound

https://huagongshe.com/reaction/1177419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzoic acidHCID 57394406—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductHCID 59174896HCID 59174896—

Reaction Steps

3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)benzoic acid (107 mg, 0.274 mmol) was dissolved in thionyl chloride at 65° C. for 1 h before it was concentrated. The reaction mixture was dissolved in THF (1.4 mL) before ammonium hydroxide (1.07 mL, 27.40 mmol) was added and stirred at ambient temp. for 16 h. The reaction mixture was diluted with EtOAc, added to a separatory funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed with sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, and concentrated via rotovap to give the title compound after preparatory LC. MS (ESI) m/z: Calculated: 389; Observed: 390.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-49b9f9d037d04826a494baa946693f2d
Source noteuspto-grants-2010_11