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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590841Generated: October 30, 2026

4-Methoxybenzylamine → N-benzyl-1-(6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)propan-2-amine

https://huagongshe.com/reaction/590841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-chloro-3-iodo-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118168962—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductN-benzyl-1-(6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)propan-2-amineHCID 118272365—

Reaction Steps

6-chloro-3-iodo-trityl-1H-pyrazolo[4.3-c]pyridine (Intermediate 1C, 2 g, 3.73 mmol), N, N dimethylacetamide-dimethyl acetal (DMA-DMA) (4.97 g, 37.3 mmol) were stirred at 125° C. for 12 hrs. Reaction was concentrated and excess DMF-DMA azeotroped with Toluene. The resulting intermediate and p-methoxybenzylamine (2.05 g, 14.9 mmol) were stirred in a 3:1:1 solution of DCE:AcOH:EtOH (20 ml) at 85° C. for 3 hrs. Solvent was removed by vacuum and the residue was taken in DCE (15 ml) followed with addition of sodium triacetoxyborohydride (3.16 g, 14.9 mmol) and acetic acid (0.9 g, 14.9 mmol) before the mixture was stirred at room temperature for 6 hours. The reaction mixture was partitioned between DCM and aqueous sodium bicarbonate and the organics was separated, washed with brine, dried with sodium sulfate and concentrated. Purification of the residue by flash column (0-90% -EtOAc-hexanes) gave N-benzyl-1-(6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)propan-2-amine MS ESI calc'd. for C35H30ClIN4 [M+H]+ 700. found 700.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-6f65678903ce46e99ca606cc88ed4335
Source noteuspto-grants-2016_01