HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424151Generated: October 30, 2026
HCID 178458084, compound → HCID 178461774, compound
https://huagongshe.com/reaction/1424151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178458084 | HCID 178458084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 178461774 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927587B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-f8e4410515824993a3c0708f9d70f99c |
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| Source note | uspto-grants-2015_01 |
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