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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373187Generated: October 31, 2026

2-Methylbenzaldehyde → HCID 58780951, compound

https://huagongshe.com/reaction/1373187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 58780935HCID 58780935—
SolventMethanolHCID 887—
ProductHCID 58780951HCID 5878095196%

Reaction Steps

2-Methylbenzaldehyde (0.035 ml, 0.3 mM) was added to a solution of 2-[3-amino-5-(4-methyl-thiazol-5-yl) ethoxy benzoyl]amino-5-pyridine carboxylic acid (0.10 g 0.25 mM) and 4A molecular sieves (0.25 g) in methanol (15 ml), under an inert atmosphere at room temperature. After 1 hr sodium cyanoborohydride (0.019 g, 0.3 mM) was added and the reaction mixture stirred for 40 hrs. The reaction mixture was filtered, concentrated in vacuo, 2M NaOH added to pH=11–12 then acidified with 2M HCl to precipitate a colourless solid. The solid was filtered, washed with water to give the title compound as a colourless solid (0.12 g, 96%); 1H NMR δ (d6-DMSO): 2.33 (m, 6H), 3.19 (dd, 2H), 4.13 (dd, 2H), 4.26 (s, 2H), 6.33 (s, 1H), 6.83 (s, 1H), 6.90 (s, 1H), 7.09–7.19 (m, 3H), 7.26 (s, 1H), 8.28 (s, 2H), 8.83 (s, 1H), 8.88 (s, 1H), 10.87 (s, 1H), 13.09 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160906B2
Source datasetuspto-grants-2007_01
ORD IDord-e8c4fb89dc7e4b51980d33a6e4e838ec
Source noteuspto-grants-2007_01