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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062376Generated: November 1, 2026

HCID 874532, compound → HCID 69748795, compound

https://huagongshe.com/reaction/1062376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 874532HCID 874532—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 54333950HCID 54333950—
CatalystCuprous chlorideHCID 62652—
SolventDimethylacetamideHCID 31374—
ProductHCID 69748795HCID 6974879544.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

Copper (1) chloride (0.038 g) was added to a mixture of (R)-N-(2-chloro-4-mercaptophenyl)-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Example 210) (0.21 g), N-(4-iodobenzenesulphonyl)pyrrolidine (0.258 g) and sodium methoxide (0.042 g) in DMA (5 ml). The mixture was heated at 150° C. with stirring for 4 hours then cooled and the DMA removed by evaporation. Ethyl acetate (20 ml) and water (20 ml) was added and the mixture was filtered. The aqueous layer was extracted with ethyl acetate (3×20 ml) and the organic layers were combined and dried. Volatile material was removed by evaporation and the residue was purified on a silica gel Mega Bond Elut column, eluting with methanol/DCM 0-10% to give the title compound (0.16 g) as a solid. NMR (CDCl3): 1.75 (s, 3H), 1.75-1.85 (m, 4H), 3.2-3.3 (m, 4H), 4.0 (s, 1H), 7.2-7.3 (m, 2H), 7.4-7.45 (m, 1H), 7.6 (s, 1), 7.7 (d, 2H), 8.45 (d, 1H), 9.15 (s, 1H); MS (ESP−): 507.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960688B2
Source datasetuspto-grants-2005_11
ORD IDord-acd0253acaae4a3d8aaba5c09bd405f7
Source noteuspto-grants-2005_11