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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458768Generated: October 30, 2026

Phenol → (7R,9aS)-7-Phenoxymethyl-2-pyrimidin-2-yl-octahydro-pyrido[1,2-a]pyrazine

https://huagongshe.com/reaction/1458768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactantcis-(2-Pyrimidin-2-yl-octahydro-pyrido[1,2-a]pyrazin-7-yl)-methanolHCID 14995231—
SolventTetrahydrofuranHCID 8028—
Product(7R,9aS)-7-Phenoxymethyl-2-pyrimidin-2-yl-octahydro-pyrido[1,2-a]pyrazineHCID 1581741061.6%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of 0.385 g (1.55 mmol) of (7R,9aS)-7-hydroxymethyl-2-(pyrimidin-2-yl)-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (Preparation 4), 0.220 g (2.34 mmol) of phenol, and 0.488 g (1.86 mmol) of triphenylphosphine in 30 mL of dry THF was treated with 0.324 g (1.86 mmol) of diethyl azodicarboxylate, and the mixture stirred at 23° C. for 16 h. The solvent was evaporated, the residue dissolved in ethyl ether and treated with HCl(g) in ether. The precipitate was collected on a Buchner funnel, and washed with 1:1 ether:ethyl acetate three times. The solid was dissolved in water, basified with 1M NaOH and extracted with chloroform. The organic layer was washed with 1M NaOH (2×) and water (1×), dried (magnesium sulfate), filtered and evaporated to give 0.310 g of (7R,9aS)-7-phenoxymethyl-2,3,4,6,7,8,9,9a-octahydro-2-pyrimidin-2-yl-1H-pyrido[1,2-a]pyrazine. mp (.HCl) 203°-205° C. 13C NMR (base, CDCl3): δ 27.0, 29.0, 36.4, 43.6, 49.1, 54.9, 58.8, 60.8, 70.9, 109.8, 114.5, 120.6, 129.4, 157.7, 159.0, 161.5. HRMS calcd for C19H24N4O: 324.195. Found: 324.194.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852031
Source datasetuspto-grants-1998_12
ORD IDord-096ad3b7195940b7aeb30d4205266167
Source noteuspto-grants-1998_12