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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396864Generated: November 2, 2026

Pyridine → (2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoyl fluoride

https://huagongshe.com/reaction/1396864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant(2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoic acidHCID 11185069—
SolventDichloromethaneHCID 6344—
Product(2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoyl fluorideHCID 86706342100%

Reaction Steps

To a solution of (2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)hexanoic acid (9) (1.7 g, 6.1 mmol) in DCM (20 mL) was added pyridine (0.53 g, 6.7 mmol), followed by 2,4,6-trifluoro-1,3,5-triazine (0.86 g, 6.4 mmol) dropwise. The reaction mixture was stirred for 4 h and TLC indicated completion of the reaction. The reaction mixture was washed with 10% aqueous citric acid and brine, dried over Na2SO4, and concentrated to provide the title compound (1.7 g, 100%) as red oil. 1H NMR (300 MHz, DMSO) δ ppm 0.86 (t, J=6.7 Hz, 3H), 1.16-1.38 (m, 4H), 1.57 (m, 2H), 3.03 (m, 1H), 3.87 (m, 2H), 4.91 (s, 2H), 7.41 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-13737076165644e5a45aac3e696ee427
Source noteuspto-grants-2014_12