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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521405Generated: October 30, 2026

Tetrahydrofuran → HCID 44480583, compound

https://huagongshe.com/reaction/1521405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 66937416HCID 66937416—
SolventWaterHCID 962—
ProductHCID 44480583HCID 4448058387.8%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 1-[5-chloro-6-(propane-2-sulfonyl)-1H-benzoimidazol-2-yl]-1H-pyrazole-4-carboxylic acid ethyl ester (0.179 mg, 0.451 mmol), THF (1.7 mL), and water (0.55 mL) was added LiOH.H2O (56.8 mg, 1.35 mmol). The mixture was sonicated briefly, and stirred at 23° C. for 56 h. The solvent was evaporated, water was added, and the resulting solution was acidified to pH 1 with 1M aq. HCl. The precipitate was collected to yield the titled compound (0.146 g, 86% yield). MS (ESI/CI): mass calcd. for C14H13ClN4O4S, 368.0; m/z found, 369.0 [M+H]+. 1H NMR (600 MHz, DMSO-d6, tautomeric broadening): 14.07 (s, 1H), 13.03 (s, 1H), 8.95 (d, J=0.4 Hz, 1H), 8.36 (s, 1H), 8.16 (s, 1H), 8.09-7.64 (m, 1H), 3.88-3.76 (m, 1H), 1.22 (d, J=7.9 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073923B2
Source datasetuspto-grants-2015_07
ORD IDord-ad367f82e6b64eeb97b1db75c21ae7f3
Source noteuspto-grants-2015_07