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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965098Generated: October 25, 2026

Isopropanol → 6'-(3-Fluoropropoxy)-4-methoxy-5''-methyl-3'H-dispiro[cyclohexane-1,2'-indene-1',2''-imidazole]-4''(3''H)-thione

https://huagongshe.com/reaction/1965098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantTrimethyl orthoformateHCID 9005—
Reactant2-OxopropanethioamideHCID 20765237—
Reactant6'-(3-Fluoropropoxy)-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-imineHCID 67979550—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
Product6'-(3-Fluoropropoxy)-4-methoxy-5''-methyl-3'H-dispiro[cyclohexane-1,2'-indene-1',2''-imidazole]-4''(3''H)-thioneHCID 8666727264%

Reaction Conditions

Temperature60 °C

Reaction Steps

6′-(3-Fluoropropoxy)-4-methoxyspiro[cyclohexane-1,2′-inden]-1′(3′H)-imine (Example 20v, Step 2, 204 mg, 0.67 mmol), trimethyl orthoformate (0.193 mL, 1.76 mmol) and 2-propanol (5 mL) was added to a MW vial. The vial was sealed and the mixture was heated at 60° C. (oil bath). 2-Oxopropanethioamide (Intermediate 2, 138 mg, 1.34 mmol) in MeOH (15 mL) was added and the resulting mixture was stirred overnight at 60° C. and was then concentrated in vacuo. The product was isolated using flash chromatography (0-50% EtOAc in heptane) to give the title compound (167 mg, 64% yield): MS (ES+) m/z 391 [M+H]1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415483B2
Source datasetuspto-grants-2013_04
ORD IDord-46bca9673c0c41a2babfd339cb3e1cba
Source noteuspto-grants-2013_04