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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59774Generated: October 29, 2026

(1,3,5-trimethyl-1H-pyrazol-4-yl)methylamine → [4-(2-o-Tolyl-chroman-6-yloxy)-cyclohexyl]-(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-amine

https://huagongshe.com/reaction/59774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,3,5-trimethyl-1H-pyrazol-4-yl)methylamineHCID 2776430—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 90389985HCID 90389985—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product[4-(2-o-Tolyl-chroman-6-yloxy)-cyclohexyl]-(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)-amineHCID 9039029795.7%

Reaction Steps

To a solution of 100 mg 4-(2-o-tolyl-chroman-6-yloxy)-cyclohexanone (0.30 mmol) in 2 ml of methanol and 0.15 ml of acetic acid at room temperature 124 mg (1,3,5-trimethyl-1H-pyrazol-4-yl-methyl)amine (0.89 mmol) and 56 mg of sodium cyanoborohydride (0.89 mmol) were added in one portion and stirring at room temperature was continued for 2 h. Volatile components were removed under reduced pressure and the resulting residue dissolved in dichloromethane. The organic layer was washed with aqueous 2N sodium hydroxide solution and saturated aqueous sodium chloride solution. The organic layer was dried with sodium sulfate and filtered, and the solvent removed under reduced pressure. The crude product was purified by reversed phase HPLC. 132 mg of the title compound were isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440941B2
Source datasetuspto-grants-2016_09
ORD IDord-bc102e7b04324135b795bff309f724c0
Source noteuspto-grants-2016_09