Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478643Generated: October 26, 2026

1-Azido-3,5-bis(trifluoromethyl)benzene → (2S,3S)-ethyl-3-((S)-1-((1-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,3-triazol-4-yl)methylamino)-1-oxo-3-(thiazol-4-yl)propan-2-ylcarbamoyl)oxirane-2-carboxylate

https://huagongshe.com/reaction/1478643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Azido-3,5-bis(trifluoromethyl)benzeneHCID 13106095—
ReactantTributyltin acetateHCID 16682741—
Reactant(2S,3S)-ethyl-3-((S)-1-oxo-1-(prop-2-ynylamino)-3-(thiazol-4-yl)propan-2-ylcarbamoyl)oxirane-2-carboxylateHCID 71817782—
CatalystDimethylformamideHCID 6228—
CatalystCopper SulfateHCID 24462—
SolventHCID 86659795HCID 86659795—
Product(2S,3S)-ethyl-3-((S)-1-((1-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,3-triazol-4-yl)methylamino)-1-oxo-3-(thiazol-4-yl)propan-2-ylcarbamoyl)oxirane-2-carboxylateHCID 13173651487.8%

Reaction Steps

The general click procedure was used substituting the following quantities using: 37 (93.7 mg, 0.27 mmol); 1-azido-3,5-bis(trifluoromethyl)benzene (82.5 mg, 0.32 mmol); CuSO4 (0.6 mg, 0.01 mmol); NaAsc (3.5 mg, 0.02 mmol); TBTA (15.0 mg, 0.03 mmol); in t-BuOH/EtOH/H2O (4:4:2) with an additional 3 drops of DMF; afforded the 43 as a while solid (142 mg, 87.8%). 1H NMR (CDCl3, 400 MHz): δ 8.77 (s, 1H); 8.25 (s, 2H); 8.09 (s, 1H): 7.96 (s, 1H); 7.77-7.75 (d, 1H, J=7.09 Hz); 7.34-7.32 (t, 1H); 7.11 (s, 1H); 4.81-4.76 (q, 1H); 4.59-4.57 (d, 2H, J=5.90 Hz); 4.31-4.25 (m, 2H); 3.72-3.711 (d, 1H, J=1.64 Hz); 3.55-3.54 (d, 1H, J=1.64 Hz); 3.41-3.17 (m, 2H); 1.01-0.99 (t, 3H). 13C NMR (DMSO-d6, 100 MHz): 170.62, 167.49, 165.37, 154.06, 153.24, 146.92, 138.31, 124.57, 122.37, 121.85, 121.09, 116.21, 61.97, 53.44, 52.97, 51.74, 34.64, 33.49, 14.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403843B2
Source datasetuspto-grants-2016_08
ORD IDord-32520ed271ee44b89c48cfda50ff59e4
Source noteuspto-grants-2016_08