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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486591Generated: October 28, 2026

Sodium cyanoborohydride → N*3*-(3,5-Dichloro-phenyl)-N*5*-(1-methanesulfonyl-piperidin-4-yl)-1H-[1,2,4]triazole-3,5-diamine

https://huagongshe.com/reaction/1486591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(Methylsulphonyl)piperidin-4-oneHCID 12072029—
Reactant3-Amino-5-(3,5-dichloroanilino)-s-triazoleHCID 72714614—
Reactant2,6-Dichloro-4-isothiocyanatobenzonitrileHCID 86707600—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN*3*-(3,5-Dichloro-phenyl)-N*5*-(1-methanesulfonyl-piperidin-4-yl)-1H-[1,2,4]triazole-3,5-diamineHCID 1785049488%

Reaction Steps

To a stirred solution of N3-(3,5-dichlorophenyl)-1H-1,2,4-triazole-3,5-diamine Intermediate 2 (122 mg, 0.50 mmol) in methanol (8 mL) at rt, was added 1-(methylsulfonyl)piperidin-4-one (89 mg, 0.50 mmol). The mixture was stirred for 2 hrs, after which, sodium cyanoborohydride (94.2 mg, 1.5 mmol) and three drops of acetic acid were added. The reaction mixture was stirred at rt for 6 hrs, then diluted with water (25 mL) and extracted with EtOAc (3×10 mL). The extracts were dried with sodium sulfate and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column to give 16 mg (8%) of desired product as a white solid. MS +m/z: 404.9 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428469B2
Source datasetuspto-grants-2016_08
ORD IDord-35ea24d76d614e88b3802581edf5bb1a
Source noteuspto-grants-2016_08