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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713092Generated: November 1, 2026

Sodium Iodide → 2-[2-(4-Cyclobutyl-piperazin-1-yl)-2-oxo-ethyl]-1,2,3,4-tetrahydro-isoquinoline-7-carboxylic acid methylamide

https://huagongshe.com/reaction/1713092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-1,2,3,4-tetrahydroisoquinoline-7-carboxamideHCID 57479413—
Reactant2-Chloro-(4-cyclobutyl-piperazine) acetamideHCID 66877902—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-[2-(4-Cyclobutyl-piperazin-1-yl)-2-oxo-ethyl]-1,2,3,4-tetrahydro-isoquinoline-7-carboxylic acid methylamideHCID 59463538—

Reaction Steps

To a stirred solution of 1,2,3,4-tetrahydro-isoquinoline-7-carboxylic acid methylamide (96 mg, 0.5 mmol) in acetonitrile (3.0 ml) is added 2-chloro-(4-cyclobutyl-piperazine)-acetamide (109 mg, 0.5 mmol, 1.0 eq.), K2CO3 (138 mg, 1.0 mmol, 2.0 eq.), and NaI (10 mg). The resulting mixture is stirred at rt overnight. Water (10.0 ml) is added to quench the reaction, and the acetonitrile is evaporated. The residue is extracted with DCM (10 ml×3), and the combined organic phase is dried over sodium sulfate and concentrated. The residue is purified by PTLC (EtOAc/4% TEA plus 4% EtOH) to give the title compound. MS (+VE) m/z 371.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795262B2
Source datasetuspto-grants-2010_09
ORD IDord-6f2e90cbc2974026a0b23207e1508234
Source noteuspto-grants-2010_09