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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711350Generated: November 2, 2026

Triphosgene → HCID 89771165, compound

https://huagongshe.com/reaction/711350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantHCID 89771121HCID 89771121—
ReactantHCID 89771122HCID 89771122—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
ProductHCID 89771165HCID 8977116549.4%

Reaction Steps

To a solution of triphosgene (72 mg, 0.242 mmol) in EtOAc (5 mL) at 0° C. was added solution of (1S,8aS)-1-o-tolylhexahydropyrrolo[1,2-a]pyrazin-6(7H)-one (112 mg, 0.484 mmol), DMAP (6.2 mg, 0.05 mmol) and TEA (151 mg, 1.5 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-1-(3-isopropyl-5-(trifluoromethyl)phenyl)-N-methylethanamine (142 mg, 0.58 mmol) in EtOAc (10 mL) and TEA (151 mg, 1.5 mmol). The reaction was then stirred at 50° C. for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The combined organic layer was washed with 1 N aqueous HCl solution, dried over anhydrous Na2SO4 and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH=20/1 to 10/1) to give the title compound (60 mg, yield: 25%) as yellow solid. 1H-NMR (400 MHz, CDCl3) δ ppm 7.37 (s, 1H), 7.27 (d, J=6 Hz, 2H), 7.15 (m, 5H), 5.48 (m, 1H), 4.08 (m, 2H), 3.71 (m, 1H), 2.87 (m, 4H), 2.67 (s, 3H), 2.56 (s, 3H), 2.37 (m, 2H), 1.82 (m, 1H), 1.64 (m, 1H), 1.35 (d, 3H), 1.22 (m, 3H); m/z (ES+): 502 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181259B2
Source datasetuspto-grants-2015_11
ORD IDord-067ed7e02c4444378897c5f731893b60
Source noteuspto-grants-2015_11