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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060803Generated: November 1, 2026

Dichloromethane → HCID 57504937, compound

https://huagongshe.com/reaction/2060803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57504939HCID 57504939—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 57504937HCID 57504937—

Reaction Steps

To a solution of tert-butyl 8a-(2,4-difluoro-5-(pyrimidin-5-yl)phenyl)-4,4a,5,7,8,8a-hexahydropyrano[4,3-d][1,3]thiazin-2-ylcarbamate (0.258 g, 0.558 mmol) in CH2Cl2 (8 mL) is added TFA (4 mL) and the reaction is stirred at room temperature for 1 hour. The solvent is removed under reduced pressure to afford a residue that is diluted with water and 1 N NaOH to adjust the pH to 12. The aqueous layer is extracted three times with EtOAc. The organic layer is dried over Na2SO4 and the crude product is purified by silica gel chromatography eluting with a linear gradient of 1% to 10% 7 N NH3/MeOH in CH2Cl2 to afford the title compound as the freebase (0.165 g, 68%). The freebase (0.162 g, 0.448 mmol) is dissolved in CH2Cl2 and treated with of 1 M HCl in Et2O (0.94 mL, 0.940 mmol) and the solvent is removed under reduced pressure to afford the title compound (0.208 g, 86%). ES/MS m/e: 363 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278441B2
Source datasetuspto-grants-2012_10
ORD IDord-191ebf38d78b4441a4a20e7037fd8bce
Source noteuspto-grants-2012_10