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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109074Generated: October 30, 2026

Ammonium → HCID 11369963, compound

https://huagongshe.com/reaction/2109074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniumHCID 223—
ReactantPyridineHCID 1049—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantN-[4-Cyano-3-(trifluoromethyl)phenyl]-N-(cyclopropylmethyl)glycineHCID 11369986—
SolventAcetonitrileHCID 6342—
ProductHCID 11369963HCID 1136996340%

Reaction Steps

A mixture of N-[4-cyano-3-(trifluoromethyl)phenyl]-N-(cyclopropylmethyl)glycine (0.298 g, 1 mmol), di-tert-butyl dicarbonate (0.436 g, 2 mmol), pyridine (0.100 g, 1.25 mmol), and ammonium hydrocarbonate (0.160 g, 2.25 mmol) was stirred for 24 h in acetonitrile (8 mL). The solvent was removed under reduced pressure, then water (10 mL) was added to the residue. The resulting solid was filtered, washed with water (3×5 mL), and then dried. After drying, the solid was suspended in diethyl ether (10 mL) and stirred for 12 h. The mixture was filtered, washed with diethyl ether (5 mL), and dried to obtain 0.118 g (40%) of the title compound as a white solid: 1H NMR (400 MHz, CDCl3) δ 7.63 (d, J=8.6 Hz, 1H), 7.03 (d, J=2.3 Hz, 1H), 6.84 (dd, J=8.8, 2.5 Hz, 1H), 6.02 (bs, 1H), 5.57 (bs, 1H), 4.10 (s, 2H), 3.38 (d, J=6.6 Hz, 2H), 1.08 (m, 1H), 0.67 (m, 2H), 0.33 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514470B2
Source datasetuspto-grants-2009_04
ORD IDord-d593c938c25047819e526f532d52d981
Source noteuspto-grants-2009_04