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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880573Generated: October 31, 2026

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → HCID 67485878, compound

https://huagongshe.com/reaction/1880573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantTert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
ReactantHCID 67486117HCID 67486117—
SolventDimethylformamideHCID 6228—
ProductHCID 67485878HCID 67485878—

Reaction Steps

To a DMF solution (2 mL) of the intermediate from Step D (35 mg, 0.08 mmol) was added tert-butyl β-alaninate hydrochloride (30 mg, 0.16 mmol) DIEA (0.06 mL, 0.35 mmol) and BOP (53 mg, 0.12 mmol). The solution was stirred at room temperature for ca. 30 minutes. The solution was then partitioned between ethyl acetate and aqueous 1N HCl. The organic phase was washed with aqueous 1N HCl (3×), brine; dried over MgSO4 and filtered to give tert-butyl N-{4-[({3-[4-(trifluoromethoxy)phenyl]-1-naphthyl}oxy)methyl]benzoyl}-β-alaninate. LCMS1 4.50 min. (M+H)=566. The tert butyl group was removed by treatment with 1/1 DCM/TFA for 1 hour. The crude acid was purified by reverse phase HPLC to give the title compound. 1H NMR (500 MHz, CD3OD): δ 8.57 (s, 1H); 8.31 (d, J=8.1 Hz, 1H); 7.92 (m, 1H); 7.89 (d, J=8.3 Hz, 2H); 7.82 (d, J=8.7 Hz, 2H); 7.70 (m, 3H); 7.56-7.49 (m, 2H); 7.39 (d, J=8.1 Hz, 2H); 7.24 (s, 1H); 5.46 (s, 2H); 3.69-3.65 (m, 2H); 2.68-2.66 (m, 2H). LCMS1 3.97 min. (M+H)=510

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318760B2
Source datasetuspto-grants-2012_11
ORD IDord-21bcabf56efd45c5bef23cdf2fe3a47b
Source noteuspto-grants-2012_11