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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885692Generated: October 30, 2026

Sodium Iodide → HCID 11948442, compound

https://huagongshe.com/reaction/885692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant874804-29-2HCID 16227189—
Reactant2-(6-Methoxy-[1,5]naphthyridin-4-yl)4,5,6,7-tetrahydro-2H-indazol-5-ylamineHCID 59560648—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 11948442HCID 1194844264.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-(6-methoxy-[1,5]naphthyridin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamine (30 mg, 0.1 mmol) in DMF (1 mL) were added K2CO3 (40 mg, 0.3 mmol) and 2-chloro-N-(3,5-difluoro-phenyl)-acetamide (20 mg, 0.1 mmol), and the mixture was stirred for 15 h. A catalytic amount of NaI was added and the mixture heated at 50° C. for 15 h. The mixture was diluted with EtOAc (25 mL), washed with brine (4×10 mL), dried (MgSO4) and concentrated. The resulting residue was purified on SiO2 (0-5% CH3OH/CH2Cl2) to provide 30 mg (64%) of the title compound as a pale yellow solid. MS (ESI): exact mass calculated for C24H22F2N6O2, 464.18; m/z found, 465.3 [M+H]+. 1H NMR (500 MHz, CDCl3): 9.30 (br s, 1H), 9.08 (s, 1H), 8.76 (d, J=9.2, 1H), 8.24 (d, J=5.9, 1H), 8.19 (d, J=5.1, 1H), 7.15 (d, J=9.1, 1H), 6.93-6.87 (m, 2H), 6.26 (tt, J=8.9, 2.3, 1H), 3.89 (s, 3H), 3.59 (d, J=17.7, 1H), 3.36 (d, J=17.7, 1H), 3.26-3.23 (m, 1H), 3.08-3.02 (m, 1H), 2.93-2.85 (m, 2H), 2.62 (dd, J=15.7, 5.7, 1H), 2.12-2.08 (m, 1H), 2.00-1.96 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242275B2
Source datasetuspto-grants-2012_08
ORD IDord-7b0958712dd74216846f0a29d35d9814
Source noteuspto-grants-2012_08