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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220902Generated: October 29, 2026

Triethylamine → HCID 57555403, compound

https://huagongshe.com/reaction/220902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67287955HCID 67287955—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 57555403HCID 5755540395%

Reaction Steps

(1-Benzyl-2-methyl-4,5-dihydro-1H-1,3,6-triaza-benzo[e]azulen-6-yl)-[3-fluoro-4-(3-piperazin-1-yl-propoxy)-phenyl]-methanone dihydrochloride from Example E69.2 (105 mg, 0.17 mmol) was dissolved in methanol (2.45 ml) and triethylamine (0.07 ml, 0.50 mmol). Acetic acid (0.05 ml) then 3,3-dimethylbutyraldehyde (0.032 ml, 0.25 mmol) were added and the mixture was stirred for 1 h at room temperature. Sodium cyanoborohydride (16 mg, 0.25 mmol) was added and the mixture was stirred for 3 h at room temperature then concentrated in vacuo. The residue was dissolved in dichloromethane, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 5% methanol:95% dichloromethane) to yield the title compound (102 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-b656986885204794b72f2b5c10de10d7
Source noteuspto-grants-2012_06