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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817116Generated: November 1, 2026

Lithium Hydroxide → HCID 68419598, compound

https://huagongshe.com/reaction/1817116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 68421046HCID 68421046—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 68419598HCID 6841959883.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 16 g of 4-{1-[2-(4-Acetyl-3,5-dimethyl-piperazin-1-yl)-pyridin-4-yl]-1H-[1,2,4]triazol-3-ylamino}-benzoic acid ethyl ester (34.5 mMol, 1.00 equiv) in 200 mL of 1:1 MeOH:THF was added 5.75 g of lithium hydroxide (137 mMol, 4.00 equiv) in 100 mL of water. The solution was stirred at 60° C. for 12 hr and then the MeOH and THF were removed via rotary evaporation. The basic solution was neutralized by the addition of 68 mL of 2N HCl and the precipitate was isolated by filtration, yielding 12.5 g of 4-{1-[2-(4-Acetyl-3,5-dimethyl-piperazin-1-yl)-pyridin-4-yl]-1H-[1,2,4]triazol-3-ylamino}-benzoic acid (28.7 mMol 83.5% yield) as a yellow solid. 1H NMR (500 MHz, DMSO-d6) ∂ 10.215 (1H, s), 9.48 (1H, s), 8.18 (1H, d), 7.91 (2 h, d), 7.71 (2H, d), 7.49 (1H, s), 7.35 (1H, d), 4.38 (2H, m), 3.31 (4H, m), 2.10 (3H, s), 1.22 (6H, m) ppm. LC/MS: 2.02 min/436.30 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598245B2
Source datasetuspto-grants-2009_10
ORD IDord-0609f7f56aa04e988e4d9e34d573a134
Source noteuspto-grants-2009_10