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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247764Generated: October 30, 2026

Pyridine → 620627-47-6

https://huagongshe.com/reaction/1247764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantN-[(1R)-2-Hydroxy-2-methyl-1-phenylpropyl]-4-methylbenzene-1-sulfonamideHCID 26596944—
SolventTetrahydrofuranHCID 8028—
Product620627-47-6HCID 5735159787.5%

Reaction Steps

To a solution of (1R)-N-(2-hydroxy-2-methyl-1-phenyl-propyl)-4-methyl-benzene sulfonamide (2.0 g, 6.3 mmol) in THF 8 mL at −45° C. was added SOCl2 (1.12 g, 9.4 mmol), followed by slow addition of pyridine (1.24 g, 12.9 mmol) in THF (8 mL) over a period of 2 h. The reaction was monitored on TLC. The reaction was quenched by addition of saturated aqueous NaHCO3 and the mixture was extracted with EtOAc (30 ml), and organic phase washed with brine (20 mL) and evaporated to dryness. The residue was added hexane (40 mL) and stirred at ambient for 2 h. The precipitate formed was filtered and wet cake washed with hexane to afford the title compound (2.0 g, 87.5%) with 99% de.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129378B2
Source datasetuspto-grants-2006_10
ORD IDord-53f2a83448b942aab60d991a2c572bc7
Source noteuspto-grants-2006_10