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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482361Generated: November 2, 2026

Bromoacetonitrile → HCID 89668645, compound

https://huagongshe.com/reaction/1482361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Azido-N-Boc-L-NorvalineHCID 23629197—
SolventAcetonitrileHCID 6342—
ProductHCID 89668645HCID 89668645107.1%

Reaction Steps

N,N-Diisopropylethylamine (111 μL, 0.639 mmol) and subsequently bromoacetonitrile (203 μL, 2.90 mmol) were added to a solution of (S)-5-azido-2-((tert-butoxycarbonyl)amino)pentanoic acid (Compound tk69) (150 mg, 0.581 mmol) in acetonitrile (0.8 mL) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred at the same temperature for 4 hours and then concentrated under reduced pressure, and the resulting crude product was purified by normal-phase silica gel column chromatography (hexane/ethyl acetate) to afford (S)-cyanomethyl 5-azido-2-((tert-butoxycarbonyl)amino)pentanoate (Compound tk70) (185 mg, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409952B2
Source datasetuspto-grants-2016_08
ORD IDord-1858c5d6c5234488811f433b34c10c74
Source noteuspto-grants-2016_08