Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201545Generated: October 29, 2026

Lithium hydroxide, monohydrate → HCID 117771339, compound

https://huagongshe.com/reaction/2201545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 117771053HCID 117771053—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 117771339HCID 11777133999%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 3-(benzyloxy)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)picolinate (540 mg, 0.87 mmol), LiOH.H2O (110 mg, 2.62 mmol) in 1,4-dioxane/H2O (15 mL/5 mL) under N2 was stirred at 100° C. for 1 h. After being filtrated and acidified with HCl to pH=5, the mixture was extracted with EtOAc, the organic phases were dried and concentrated to afford 3-(benzyloxy)-6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)picolinic acid (520 mg, yield: 98%). 1H-NMR (DMSO-d6, 400 MHz) δ 8.56 (d, J=4.8 Hz, 1H), 7.94˜8.07 (m, 3H), 7.73˜7.85 (m, 3H), 7.50 (d, J=7.2 Hz, 2H), 7.42 (t, J=7.6 Hz, 4H), 7.35 (br s, 1H), 5.30 (s, 2H), 3.20 (s, 3H), 2.94 (s, 3H), 2.82 (d, J=4.4 Hz, 3H). MS (M+H)+: 604.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-47a34655f03c4e0482c2c6c17f9f801b
Source noteuspto-grants-2016_06