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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384042Generated: October 31, 2026

Tetrahydrofuran → HCID 86651622, compound

https://huagongshe.com/reaction/384042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 86651623HCID 86651623—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86651622HCID 8665162296%

Reaction Conditions

Temperature50 °C

Reaction Steps

Methyl (5R,7R)-8-{[{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}(methyl)amino]carbonyl}-7-(4-fluoro-2-methylphenyl)-1,8-diazaspiro[4.5]decane-4-carboxylate (Intermediate 41, 12 mg, 0.020 mmol) was dissolved in Methanol (0.3 ml) and Water (0.3 ml). To the mixture was added LiOH H2O (0.918 mg, 0.022 mmol) and the reaction mixture was left stirring overnight at 50° C. To the solution was added Tetrahydrofuran (THF) (0.3 ml) and it was heated at 70° C. for 1 more hour. The solvent was removed in vacuo obtaining the title compound (11.2 mg, 0.019 mmol, 96% yield); 1H NMR (400 MHz, DMSO-d6) δ ppm 7.98 (s, 1H) 7.69 (s, 2H) 7.07-7.15 (m, 1H) 6.84-6.91 (m, 1H) 6.69-6.79 (m, 1H) 5.25-5.38 (m, 1H) 4.43 (d, 1H) 2.98-3.23 (m, 2H) 2.69 (s, 3H) 2.60-2.92 (m, 2H) 2.31 (s, 3 H) 1.56-2.04 (m, 5H) 1.48 (d, 3H) 1.40-1.54 (m, 1H) 1.33 (d, 1H). Stereochemistry consistent with the following data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367692B2
Source datasetuspto-grants-2013_02
ORD IDord-f3e3969b8f904e619782027100d0cbe6
Source noteuspto-grants-2013_02