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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749020Generated: October 30, 2026

Triethylamine → HCID 69108648, compound

https://huagongshe.com/reaction/749020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 69113715HCID 69113715—
SolventDichloromethaneHCID 6344—
ProductHCID 69108648HCID 6910864892%

Reaction Steps

Acid compound 46 (1.2 g, 2.73 mmol) was dissolved in DCM (30 mL). Triethylamine (0.46 mL, 3.27 mmol) and BOP reagent (1.33 g, 3.0 mmol) were added and the reaction mixture stirred at room temperature for 15 min under an atmosphere of argon. Ammonia gas was then bubbled gently through the solution for 15-20 min to complete the reaction. Excess ammonia was degassed, the solvent was removed under reduced pressure and the residue was suspended in EtOAc (75 mL). The organic layer was washed with 0.5 N NaOH (2×10 mL), water (2×25 mL), and brine (1×30 mL), dried and concentrated under reduced pressure to yield the amide compound 51 (1.1 g, 92%). 1H NMR (DMSO-d6): 7.54 (d, J=8.0 Hz, 4H), 7.31 (d, J=8.0 Hz, 2H), 7.27 (d, J=8.4 Hz, 2H), 7.09 (d, J=8.4 Hz, 1H), 6.77 (br, 1H), 4.56 (m, 1H), 2.93 (s, 3H), 2.75-2.90 (m, 7H), 2.74 (t, J=8.4 Hz, 2H), 1.30 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399786B2
Source datasetuspto-grants-2008_07
ORD IDord-f592b8f200c74d71b7f389b3c02025cb
Source noteuspto-grants-2008_07