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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590842Generated: October 30, 2026

Tetrahydrofuran → 7-Chloro-3-(4-methoxybenzyl)-4-methyl-1,3,4,5-tetrahydropyrazolo[3,4,5-de][1,6]naphthyridine

https://huagongshe.com/reaction/590842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium t-butoxideHCID 23676156—
ReactantN-benzyl-1-(6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)propan-2-amineHCID 118272365—
Catalyst2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
SolventEthyl AcetateHCID 8857—
Product7-Chloro-3-(4-methoxybenzyl)-4-methyl-1,3,4,5-tetrahydropyrazolo[3,4,5-de][1,6]naphthyridineHCID 118271792—

Reaction Conditions

Temperature55 °C

Reaction Steps

N-benzyl-1-(6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-yl)propan-2-amine (670 mg, 0.958 mmol) and RuPhos pre-catalyst (70 mg, 0.096 mmol) were charged in a 2 dram vial, evacuated and backfilled with nitrogen and taken in toluene (4.8 mL). A solution of 2M NaOtBu in THF (1.2 ml, 2.4 mmol) was added and the reaction mixture was heated to 55° C. for 12 hours. The reaction mixture was cooled and diluted with EtOAc and washed with water, brine, dried with sodium sulfate and concentrated. Purification of the residue by flash column (0-50% EtOAc-hexanes) gave 7-chloro-3-(4-methoxybenzyl)-4-methyl-1,3,4,5-tetrahydropyrazolo[3,4,5-de][1,6]naphthyridine. MS ESI calc'd. for C35H30ClIN4 [M+H]+ 572. found 572.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-12d977be2ac84c5e931e3c600dbe2d44
Source noteuspto-grants-2016_01