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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414826Generated: November 1, 2026

Hydrochloric Acid → HCID 10143150, compound

https://huagongshe.com/reaction/2414826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant7-Methyl-[1,8]naphthyridin-4-ylamineHCID 12455201—
Reactant{2-[1-(4-fluoro-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-ethyl}-carbamic acid tert-butyl esterHCID 69763736—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 10143150HCID 10143150—

Reaction Steps

To a stirred solution of {2-[1-(4-fluoro-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-ethyl}-carbamic acid tert-butyl ester (example 106.1, 0.22 g, 0.5 mmol) in glacial AcOH (1 mL) is added conc. HCl (0.1 mL). After 5 min, the reaction mixture is partitioned with CHCl3 (20 mL) and 1 N NaOH (15 mL). The organic phase is evaporated. The residue is taken up in DMSO (2 mL) and treated with CDI (0.2 g, 0.6 mmol, 1.2 eq). The reaction mixture is stirred at rt for 3 h, and then 4-amino-7-methyl-[1,8]-naphthyridine (example C5, 0.19 g, 0.6 mmol) is added. To the resulting solution is added in a single portion NaHMDS (2 M in THF, 1.25 mL, 2.5 mmol). The reaction mixture is stirred at rt for 30 min, then H2O (0.4 mL) is added. The reaction mixture is evaporated and the residue purified by preparative HPLC to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815451B2
Source datasetuspto-grants-2004_11
ORD IDord-0ff791c0f9cb4120988598d97de24975
Source noteuspto-grants-2004_11