Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70893Generated: October 29, 2026

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → HCID 59607745, compound

https://huagongshe.com/reaction/70893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Methoxyoxazole-5-carboxylic acidHCID 55303867—
Reactant(R)-ethyl 3-amino-4-(3'-chlorobiphenyl-4-yl)butanoate hydrochlorideHCID 86648190—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59607745HCID 59607745—

Reaction Steps

To a solution of 2-methoxyoxazole-5-carboxylic acid, intermediate 16, (98 mg, 0.69 mmol) and (R)-ethyl 3-amino-4-(3′-chlorobiphenyl-4-yl)butanoate hydrochloride (210 mg, 0.57 mmol) in DMF (10 mL) and CH2Cl2 (4 mL) is added HATU (272 mg, 0.72 mmol) and TEA (0.50 mL, 3.58 mmol). The crude is stirred at room temperature for 2 hrs. The crude is quenched with water and diluted in EtOAc. The organic layer is washed with water 3×, brine, dried over MgSO4, filtered, and concentrated. The crude is purified via flash chromatography using 30% EtOAc/heptane to 70% EtOAc/heptane to give (R)-ethyl 4-(3′-chlorobiphenyl-4-yl)-3-(2-methoxyoxazole-5-carboxamido)butanoate (122 mg). HPLC retention time=1.89 minutes (condition A); MS (m+1)=443.2; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.28 (t, J=7.1 Hz, 3 H), 2.52-2.66 (m, 2 H), 2.94 (dd, 1 H), 3.08 (dd, J=13.6, 6.3 Hz, 1 H), 4.12 (s, 3 H), 4.14-4.23 (m, 2 H), 4.60-4.71 (m, 1 H), 6.81 (d, J=8.8 Hz, 1 H), 7.25-7.32 (m, 3 H), 7.35 (t, J=7.7 Hz, 1 H), 7.42 (s, 1 H), 7.43-7.47 (m, 1 H), 7.48-7.54 (m, 2 H), 7.55 (t, J=1.6 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822534B2
Source datasetuspto-grants-2014_09
ORD IDord-62b62e3c7d034023b205b327644ad223
Source noteuspto-grants-2014_09