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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079811Generated: November 1, 2026

2-Naphthalenecarboxaldehyde → HCID 49855398, compound

https://huagongshe.com/reaction/2079811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenecarboxaldehydeHCID 6201—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-[6-(aminomethyl)-3-azabicyclo[3.1.0]hex-3-yl]pyrimidine-5-carboxylateHCID 49857516—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 49855398HCID 49855398—

Reaction Steps

Ethyl 2-[6-(aminomethyl)-3-azabicyclo[3.1.0]hex-3-yl]pyrimidine-5-carboxylate (200 mg, 0.76 mmol) was stirred with 2-naphthaldehyde (119 mg, 0.76 mmol) in MeOH (10 ml) at r.t. under N2 for 16 h. NaBH4 (46 mg, 1.22 mmol) was then added and the mixture stirred for 10 min. Sat. aq. NH4Cl (20 ml) was added and the mixture stirred for 20 min. The reaction was then diluted with H2O (50 ml) and extracted with Et2O (2×100 ml). The combined organic layers were dried (MgSO4) and the solvent removed in vacuo to give the title compound as a yellow oil which was used in the next step without further purification. LCMS purity 92%, m/z 403 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932246B2
Source datasetuspto-grants-2011_04
ORD IDord-8de67212087f4628bed91103e0b3d2c3
Source noteuspto-grants-2011_04