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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352707Generated: November 2, 2026

HCID 22940600, compound → HCID 53849828, compound

https://huagongshe.com/reaction/1352707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22940600HCID 22940600—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53849828HCID 5384982897.4%

Reaction Steps

A solution of 44.4 g (122 mmol) of (7R,9aS)-2-BOC-7-(4-fluorophenoxy)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (Preparation 7) in 500 mL of trifluroacetic acid and 200 mL of water was stirred at room temperature for 16 h. The mixture was concentrated by evaporation, the residue dissolved in water, basified with 15% NaOH, and extracted with ethyl acetate (2×). The organic layers were dried (magnesium sulfate), filtered and evaporated to give 31.4 g (96%) of (7R,9aS)-7-(4-fluorophenoxy)methyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine which was suitable for use in subsequent reactions. Purification of a 0.40 g sample by flash silica gel chromatography eluting with 90:10 chloroform:methanol gave 0.38 g of colorless crystals. mp (.2 HCl) 200–201° C. 13C NMR (base, CDCl3): δ 27.2, 29.1, 36.3, 45.9, 51.9, 56.0, 59.1, 62.5, 71.7, 115.4 (d, JCF=8). 115.7 (d, JCF=23). HRMS calcd for C15H21FN2O: 264.1638, found: 264.1660.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220753B2
Source datasetuspto-grants-2007_05
ORD IDord-e562cb34bd154f19a81ebe2839136a86
Source noteuspto-grants-2007_05