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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388105Generated: October 30, 2026

HCID 57394325, compound → HCID 57396083, compound

https://huagongshe.com/reaction/388105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57394325HCID 57394325—
ReactantHCID 57403086HCID 57403086—
SolventLithium HydroxideHCID 3939—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57396083HCID 5739608390%

Reaction Steps

4-(3-(Cyclohexylmethyl)-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyrazin-5-yl)benzoic acid. A solution of methyl 4-(3-(cyclohexylmethyl)-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyrazin-5-yl)benzoate (See Example 56.A) (350 mg, 0.95 mmol) in 1N lithium hydroxide (4.5 mL) and tetrahydrofuran (4.5 mL) was allowed to stir at rt for 19 h. Upon completion of the reaction, the volatiles were removed under reduced pressure. The residue was treated with 1N hydrochloric acid and sonicated. The resulting precipitate was collected by vacuum filtration, and dried under high vacuum to afford the title compound (300 mg, 90% yield) as a tan solid. MS (ESI) m/z 353.3 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372976B2
Source datasetuspto-grants-2013_02
ORD IDord-4207a270bc8b4dcca0e55c41e866f1ba
Source noteuspto-grants-2013_02