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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373189Generated: November 1, 2026

2-Fluorobenzylamine → HCID 21074212, compound

https://huagongshe.com/reaction/1373189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorobenzylamineHCID 66649—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86594826HCID 86594826—
SolventMethanolHCID 887—
ProductHCID 21074212HCID 2107421276%

Reaction Steps

2-(3-isopropyloxy-5-carboxy-benzoyl) amino-5-pyridine carboxylic acid (0.10 g, 0.30 mM), 4A molecular sieves (0.3 g) and 2-fluorobenzylamine were stirred in MeOH at ambient temperature for 2 hrs then sodium cyanoborohydride (0.023 g, 0.36 mM) added. After a further 2 hrs the reaction mixture was filtered, residue washed with MeOH and the filtrate concentrated in vacuo. Water was added, then acidified with 2M HCl to precipitate a colourless solid which was filtered, washed with water and dried under high-vacuum to give the title compound as a light brown solid (00.10 g, 76%); 1H NMR δ (d6-DMSO): 1H NMR δ (d6-DMSO): 1.29 (d, 6H), 4.13 (d, 2H), 4.74 (m, 1H), 7.20–7.30 (m, 3H), 7.43 (m, 1H), 7.58 (m, 2H), 7.68 (s, 1H), 8.28 (s, 2H), 8.87 (s, 1H), 11.10 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160906B2
Source datasetuspto-grants-2007_01
ORD IDord-dcd142fd6e144922a567d3ef9538575a
Source noteuspto-grants-2007_01