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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657045Generated: October 30, 2026

Sodium Carbonate → Phenylmethyl ({(3S,4S)-1-[2-(7-fluoro-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl]-4-hydroxy-3-pyrrolidinyl}methyl)carbamate

https://huagongshe.com/reaction/657045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1,5-Naphthyridine-1(2H)-acetaldehyde, 7-fluoro-2-oxo-HCID 57815275—
ReactantPhenylmethyl {[(3R,4S)-4-hydroxy-3-pyrrolidinyl]methyl}carbamateHCID 59026130—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductPhenylmethyl ({(3S,4S)-1-[2-(7-fluoro-2-oxo-1,5-naphthyridin-1(2H)-yl)ethyl]-4-hydroxy-3-pyrrolidinyl}methyl)carbamateHCID 86635342—

Reaction Steps

Phenylmethyl {[(3R,4S)-4-hydroxy-3-pyrrolidinyl]methyl}carbamate (1.17 g; 4.560 mmol) and (7-fluoro-2-oxo-1,5-naphthyridin-1(2H)-yl)acetaldehyde (as the methyl hemiacetal)) (855 mg, 4.17 mmol) were combined in anhydrous DCM (5 ml) and anhydrous MeOH (1 ml) with a spatula of solid sodium carbonate. The reaction mixture was stirred under nitrogen for 1 h then sodium triacetoxyborohydride (2.76 g; 12.44 mmol) was added and stirred overnight. The reaction mixture was concentrated and the title compound was obtained as a pale yellow oil (1.69 mg, 87%) after column:chromatography (90:10: DCM:MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-d190947f996847e5b90c8756794b3941
Source noteuspto-grants-2011_12