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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966785Generated: November 1, 2026

Sodium Thiosulfate → HCID 53238529, compound

https://huagongshe.com/reaction/1966785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 58541886HCID 58541886—
Reactant4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamineHCID 58541899—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53238529HCID 5323852941.2%

Reaction Steps

To a solution of 4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamine (100 mg, 0.39 mmol) in DMF (10 mL) is added crude 5-(1,5-dimethyl-1H-pyrazol-4-yl)-2-[1,2,4]triazole-1-yl-benzaldehyde (112 mg, 0.42 mmol) at room temperature. Oxone (239 mg, 0.39 mmol) in H2O (1 mL) is added and the solution is stirred at the same temperature for 3 hours. Sat. sodium thiosulfate (10 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 (1 g) and is filtered. The filtrate is concentrated and the residue is purified by silica gel flash column chromatography with 10% MeOH in CH2Cl2 as the eluent to afford the title compound (81 mg, 41%). LCMS (ESMS): m/z: 505.40 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420655B2
Source datasetuspto-grants-2013_04
ORD IDord-1c8c490471894cebbdebc8846a9753aa
Source noteuspto-grants-2013_04