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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966692Generated: October 30, 2026

Sodium Thiosulfate → {2-Amino-5-[1-tert-butyl-2-(2-1,2,4-triazol-1-yl-phenyl)-1H-benzimidazol-5-yl]-pyridin-3-yl}-methanol

https://huagongshe.com/reaction/1966692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant2-(1H-1,2,4-Triazol-1-yl)benzaldehydeHCID 3536446—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant[2-Amino-5-(3-amino-4-tert-butylamino-phenyl)-pyridin-3-yl]-methanolHCID 58542055—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product{2-Amino-5-[1-tert-butyl-2-(2-1,2,4-triazol-1-yl-phenyl)-1H-benzimidazol-5-yl]-pyridin-3-yl}-methanolHCID 5854194510.4%

Reaction Steps

To a solution of [2-amino-5-(3-amino-4-tert-butylamino-phenyl)-pyridin-3-yl]-methanol (100 mg, 0.35 mmol) in DMF (5 mL) is added 2-[1,2,4]-triazol-1-yl-benzaldehyde (73 mg, 0.42 mmol) at room temperature. Oxone (215 mg, 0.35 mmol) in H2O (1 mL) is added and the solution is stirred for 4 hours. Saturated sodium thiosulfate solution (5 mL) is added and the mixture is extracted with EtOAc (3×10 mL) and H2O (10 mL). The combined organic layer is dried with MgSO4 and is filtered. The filtrate is concentrated and the residue is purified by silica gel flash column chromatography eluting with 10% MeOH in CH2Cl2 to afford the title compound (16 mg, 10%) as a pale brown foam. LCMS (ESMS): m/z 440.20 (M++1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420655B2
Source datasetuspto-grants-2013_04
ORD IDord-bdb04b5e2e3e4fec826fa91a277a3aa3
Source noteuspto-grants-2013_04