Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132466Generated: November 1, 2026

Methanol → HCID 178525539, compound

https://huagongshe.com/reaction/132466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 178500649HCID 178500649—
ProductHCID 178525539HCID 17852553950%

Reaction Conditions

Temperature50 °C

Reaction Steps

(S)-Methyl 2-(1,4-dichloro-8-oxo-9-(2-(piperidin-1-yl)ethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl)acetate (260 mg, 0.573 mmol) was dissolved in a mixture of tetrahydrofuran (5.0 mL, 61.6 mmol) and methanol (5.0 mL, 123 mmol). Water (5.0 mL, 278 mmol) was added to the mixture followed by lithium hydroxide hydrate (65 mg, 1.549 mmol). Mixture was warmed to 50° C. and held with stirring for 4.5 hours. Mixture was cooled to room temperature. Organic solvents were removed from the mixture by roto-vap. Residue was neutralized with 1.6 mL 1N hydrochloric acid and treated with ethyl acetate. Mixture sat at room temperature for 20 minutes allowing solids to form. Solids were filtered off and washed with water. Solids were dried in vacuo. Title compound was obtained as white solid in 50% yield. MS (M−H)−=437.1, 439.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384931B2
Source datasetuspto-grants-2008_06
ORD IDord-d0d7529829c4406e9b7786c0c0522d2c
Source noteuspto-grants-2008_06