Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201531Generated: October 29, 2026

Lithium hydroxide, monohydrate → HCID 117771171, compound

https://huagongshe.com/reaction/2201531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 117771658HCID 117771658—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 117771171HCID 11777117177%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirring solution of methyl 6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-3-methoxypicolinate (400 mg, 0.74 mmol) in dioxane/H2O (10 mL/1 mL) was added LiOH.H2O (93 mg, 2.22 mmol) under N2 protection. The mixture was stirred at 70° C. for 3 h. The mixture was concentrated in vacuo and then extracted with EtOAc. After the organic layer was washed with HCl (a.q.), brine, dried over Na2SO4, filtered and evaporated, the crude product was purified by prep-TLC (PE:EtOAc=1:3) to give the product of 6-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-(N-methylmethylsulfonamido)benzofuran-5-yl)-3-methoxypicolinic acid (300 mg, yield: 77%). 1H-NMR (Methanol-d4, 400 MHz) δ 7.86˜7.90 (m, 2H), 7.80 (s, 1H), 7.69 (s, 1H), 7.65 (s, 1H), 7.55˜7.57 (m, 1H), 7.14 (t, J=8.8 Hz, 2H), 3.83 (s, 3H), 3.04 (s, 3H), 2.86 (s, 3H), 2.82 (s, 3H). MS (M+H)+: 528.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-182bd171b94e4ed69777079bcec99a19
Source noteuspto-grants-2016_06