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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424151Generated: October 30, 2026

HCID 178458084, compound → HCID 178461774, compound

https://huagongshe.com/reaction/1424151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178458084HCID 178458084—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178461774HCID 178461774—

Reaction Steps

A solution of tert-butyl [(1S)-3-amino-1-(5-tert-butyl-1H-benzimidazol-2-yl)-2-methyl-3-oxopropyl]carbamate (Preparation 29, 3.07 g, 8.2 mmol) in DCM (50 mL) and TFA (10 mL) was stirred at room temperature for 3 hours before concentrating in vacuo. Saturated aqueous NaHCO3 solution (100 mL) was added and the product extracted with 2-MeTHF (4×100 mL). The organic layers were combined, washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified using reverse phase column chromatography eluting with 0-40% acetonitrile in water. The resulting solid was dissolved in MeCN (40 mL) at 50° C. and methanol added before allowing the solution to cool. The resulting white precipitate was collected, dried, and further triturated with EtOAc (5 mL) twice to afford a white solid as the desired (2R,3S) diastereomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927587B2
Source datasetuspto-grants-2015_01
ORD IDord-f8e4410515824993a3c0708f9d70f99c
Source noteuspto-grants-2015_01