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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783392Generated: October 27, 2026

Diisopropylethylamine → {(R)-1-[Allyl-(2,4-dimethoxy-benzyl)-carbamoyl]-but-3-enyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1783392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 4722371HCID 4722371—
ReactantO-(7-Azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium TetrafluoroborateHCID 11099301—
ReactantBoc-L-allylglycine . DCHAHCID 53395397—
SolventDimethylformamideHCID 6228—
Product{(R)-1-[Allyl-(2,4-dimethoxy-benzyl)-carbamoyl]-but-3-enyl}-carbamic acid tert-butyl esterHCID 57589913—

Reaction Steps

(R)-N-Boc-allylglycine (2.3 g, 9.9 mmol) was dissolved in dimethylformamide (20 ml) and activated with the coupling reagent TATU (3.5 g, 10.9 mmol) and Hünig's base (3.8 ml, 21.9 mmol) for 2 min. Allyl-(2,4-dimethoxy-benzyl)-amine (2.1 g, 9.9 mmol) dissolved in dimethylformamide (20 ml) was added to the chilled (ice-water bath) reaction mixture and the stirring was continued overnight. The solvent was evaporated and the residue was dissolved in ethyl acetate, washed with saturated NaHCO3 solution, 1 M KHSO4 solution, brine, dried (MgSO4.2H2O), filtered and concentrated under reduce pressure and purified over silica gel (ethyl acetate/n-heptane 1:4): colorless gum 2.6 g (62%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501406B2
Source datasetuspto-grants-2009_03
ORD IDord-8c66eddc371c43c7a53c3ee05b304da1
Source noteuspto-grants-2009_03