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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174828Generated: November 1, 2026

Water → Begacestat

https://huagongshe.com/reaction/1174828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-MethylmorpholineHCID 7972—
Reactant5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
ReactantHCID 25022953HCID 25022953—
SolventIsopropyl AcetateHCID 7915—
ProductBegacestatHCID 1126935367.8%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To a suspension of (2S)-2-amino-4,4,4-tri-fluoro-3-(trifluoromethyl)butan-1-ol (2 g, 8.1 mmol) in isopropyl acetate (10 mL), 4-methyl morpholine (2.7 mL, 24.6 mmol) was added. The mixture was stirred at 20 to 25° C. for 5 to 10 minutes and then 5-chlorothiophene-2-sulfonyl chloride (2.0 g, 9.2 mmol) was added. The reaction mixture was stirred at 20 to 25° C. for 6 to 18 hours. Water (10 mL) was added to the reaction mixture and the solid dissolved. The two layers were separated, the organic layer was washed with 10% NaHCO3 (10 mL) and 10% NaCl (10 mL), and heptane (10 mL) was added to the isopropyl acetate layer (about 10 mL). The mixture was reduced in volume by about half by distillation under atmospheric conditions. While the solution remained at 80 to 90° C., heptane (10 mL) was added over 5 to 10 minutes. A solid began to form during heptane addition. After addition, the mixture was cooled to 20 to 25° C., the solution was stirred for 1 to 2 hours, and then further cooled to 5 to 10° C. for 1 hour. The solid was collected by filtration, washed with heptane (5 mL), and oven-dried to give 2.15 g (67%) of an off-white solid. 98% area HPLC purity and >99% chiral purity by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838550B2
Source datasetuspto-grants-2010_11
ORD IDord-8c6ee9780b554c7993b00284762077f5
Source noteuspto-grants-2010_11