Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403208Generated: October 29, 2026

Triethylamine → HCID 131731438, compound

https://huagongshe.com/reaction/403208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzyloxycarbonyl-L-phenylalanineHCID 70878—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 87093237HCID 87093237—
SolventDimethylformamideHCID 6228—
ProductHCID 131731438HCID 131731438—

Reaction Steps

The (2S)-1-amino-2-tert-butyloxycarbonylamino-3-methylbutane hydrochloride was obtained from tert-butyloxycarbonyl-L-valinol in accordance with the literature procedures (Mattingly, P. G., Synthesis, 1990, 1990, 366-368. Desired Boc-protected alcohol was obtained from Boc-L-valine, in accordance with the literature procedure (Juszczyk, P. et al., Letters In Peptide Science. 2003, 10, 79-82). The solution of (2S)-1-amino-2-tert-butyloxycarbonylamino-3-methylbutane hydrochloride (0.50 g, 2.096 mmol), Z-L-phenylalanine (0.659 g, 2.20 mmol), triethylamine (611 μl, 4.4 mmol) and HOBt (0.297 g. 2.20 mmol) in 10 ml of DMF was cooled on ice bath and DCC (0.498 g, 2.42 mmol) was added in small portions, during 0.5 h. The stirring was continued during 1 hour, next the reaction mixture was left in room temperature overnight. The precipitated DCU was filtered off, washed with DMF (2×3 ml) and the combined filtrates were evaporated under reduced pressure. The solid residue was dissolved in ethyl acetate (200 ml) and the solution was washed with 1 M hydrochloric acid (3×70 ml),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748370B2
Source datasetuspto-grants-2014_06
ORD IDord-ba35cdbfbd314f51aa7396c1298e8f51
Source noteuspto-grants-2014_06