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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053809Generated: October 30, 2026

Isopropanol → (3R)-3-amino-1-(6-amino-5-fluoropyrimidin-4-yl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/1053809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium fluoride hydrateHCID 23675105—
Reactant(3R)-1-(6-amino-5-fluoropyrimidin-4-yl)-3-(((S)-1-phenylethyl)amino)piperidine-4-carboxylic acidHCID 118116588—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventWaterHCID 962—
Product(3R)-3-amino-1-(6-amino-5-fluoropyrimidin-4-yl)piperidine-4-carboxylic acidHCID 118115954—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a 10 L reaction were charged under N2, i-PrOH (3.5 L), H2O (3.5 L), 3-7 (1.0 equiv, 0.97 mol, 350 g), potassium fluoride mono hydrate (290 g, 3.0 eq, 3.0 mol) and 35 g of 20% Pd(OH)2/C (10% v/w). After evacuated/refilled with hydrogen three times, the mixture was warmed to 40-50° C. and vigorously stirred at that temperature under 1 atmosphere of hydrogen. After 18 hours, LC/MS indicated <1% of starting material 3-7 remained. The mixture was purged with N2 for 20 min, cooled to 22° C., and filtered. Both the wet cake and filtrate contained the product and processed separately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394277B2
Source datasetuspto-grants-2016_07
ORD IDord-70718b8c2892474ea98d6440dd4dd67a
Source noteuspto-grants-2016_07