Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468590Generated: November 1, 2026

Dichloromethane → HCID 45111074, compound

https://huagongshe.com/reaction/468590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonamideHCID 72879—
ReactantHCID 45110932HCID 45110932—
ProductHCID 45111074HCID 4511107471,875%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2S)-2-4-{[4-trifluoromethyl)-1,3-thiazol-2yl]amino}phenyl)propanoic acid (3) (0.1 g, 0.32 mmol) in dry CH2Cl2 (2 mL) CDI (0.055 g, 0.34 mmol) was added and the resulting solution was stirred for 1 h at T=0° C. After ice-water bath removal methanesulfonamide (0.032 g, 0.34 mmol) and TEA (40 μl, 0.29 mmol) were added and the resulting mixture was stirred at room temperature for 12 h. At the complete disappearance of the starting material, a buffer H3PO4/H2PO4− solution (pH=2.0, 5 ml) was added and the reaction mixture was trasferred into a reparatory funnel. The two phases were separated and the organic one washed with the same buffer (3×5 mL), dried over Na2SO4 and evaporated under vacuum to give a crude which was purified by flash chromatography. Pure compound 11 (0.089 g, 0.23 mol) was isolated as a yellow oil (71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08624036B2
Source datasetuspto-grants-2014_01
ORD IDord-b4f8321b20cc4027a02a04d050a1106d
Source noteuspto-grants-2014_01