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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993610Generated: October 31, 2026

2-Chlorocyclohexanone → HCID 58897199, compound

https://huagongshe.com/reaction/1993610

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorocyclohexanoneHCID 13203—
ReactantHCID 58897187HCID 58897187—
SolventMethanolHCID 887—
ProductHCID 58897199HCID 5889719911%

Reaction Steps

A solution of (S)-methyl 3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-3-thioureidopropanoate (100 mg, 0.23 mmol) and 2-chloro cyclohexanone (36 mg, 0.28 mmol) in MeOH (5.0 mL) was heated at 70° C. for 18 h. The concentrated reaction mixture was purified by silica gel ISCO chromatography (12 g column) using hexanes/EtOAc (0-30% over 15 min). (S)-methyl 3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-3-(4,5,6,7-tetrahydrobenzo[d]thiazol-2-ylamino)propanoate was isolated as a clear oil, (13 mg, 11% yield). LCMS: 1.70 min [M+1] 514.3 (2 min gradient, MeOH/H2O 0.1% TFA); HPLC: 3.65 min (4 min gradient, MeOH/H2O 0.2% PPA); Purity 96%; NMR: 400 MHz 1H (CDCl3) 8.43 ppm, 1H, d, J=2.20 Hz; 7.55 ppm, 1H, dd, J=8.57, 2.42 Hz; 7.49 ppm, 1H, s; 7.29 ppm, 2H, m; 7.14 ppm, 1H, d, J=7.91 Hz; 3.98 ppm, 1H, d, J=15.82 Hz; 3.70 ppm, 1H, d, J=15.82 Hz; 3.60 ppm, 1H, s; 3.47 ppm, 3H, s; 2.40 ppm, 4H, m; 1.68 ppm, 4H, m.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652023B2
Source datasetuspto-grants-2010_01
ORD IDord-eae285fd916f4792be44923632ca082f
Source noteuspto-grants-2010_01