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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113795Generated: November 1, 2026

Toluene → HCID 22136266, compound

https://huagongshe.com/reaction/2113795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-methoxybutan-2-oneHCID 10080345—
ReactantHCID 22136293HCID 22136293—
CatalystTitanium TetrachlorideHCID 24193—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 22136266HCID 2213626677%

Reaction Steps

2-Methyl-7-(2,4,6-trimethyl-phenyl)-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-ylamine (5-44; 101 mg, 0.373 mmol) was dissolved in CH2Cl2 (2 mL). Et3N (0.25 mL, 1.79 mmol) and the 1-methoxy-butan-2-one (65 mg, 0.636 mmol) were added at room temperature. A solution of TiCl4 in toluene (1 M; 0.35 mL, 0.35 mmol) was added dropwise via syringe. The mixture was then stirred at room temperature overnight. NaCNBH3 (120 mg, 1.9 mmol) in methanol (1 mL) was added slowly. The stirring continued at room temperature for 0.5 h and the reaction was quenched by the addition of 2 N NaOH (2 mL). EtOAc was added and the layers were separated. The organic layer was washed with water, brine and dried over MgSO4. The solvent was removed and the residue purified by chromatography on SiO2 (gradient elution: 2% MeOH in CH2Cl2 containing 0.1% NH4OH to 3% MeOH in CH2Cl2 containing 0.15% NH4OH over 20 minutes) to yield 102 mg of 5-40 (0.286 mmol; 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432283B2
Source datasetuspto-grants-2008_10
ORD IDord-6ff4fc702df94e76a191377107afc416
Source noteuspto-grants-2008_10