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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424640Generated: November 1, 2026

Sodium Iodide → HCID 58137300, compound

https://huagongshe.com/reaction/1424640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86650843HCID 86650843—
SolventAcetonitrileHCID 6342—
ProductHCID 58137300HCID 5813730018.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of (±)-7-bromo-N-(2-adamantyl)-3-(2-(p-toluenesulfonyloxy)ethyl)-2,3-dihydrospiro[indene-1,4′-piperidine]-1′-carboxamide (50 mg, 0.078 mmol) and K2CO3 (21.56 mg, 0.156 mmol) in anhydrous CH3CN (3 mL) was added NaI (3 mg, 0.020 mmol) at 0° C. Then the mixture was stirred overnight at 80-90° C. The mixture was concentrated to give the crude product which was purified by preparative HPLC to afford (±)-7-bromo-N-(2-adamantyl)-3-(2-morpholinoethyl)-2,3-dihydrospiro[indene-1,4′-piperidine]-1′-carboxamide (4 mg, 9%). LC-MS Method 5 tR=1.09 min, m/z=558; 1H NMR: (400 MHz, CDCl3): δ=1.43 (m, 2H), 1.56-1.69 (m. 3H), 1.75-1.85 (m, 9H), 1.94-2.05 (m, 3H), 2.45-2.59 (m, 4H), 2.91 (m, 2H), 3.12 (m, 5H), 3.25 (m, 2H), 3.56 (m, 3H), 3.91-4.16 (m, 6H), 4.20 (m, 2H), 7.12 (m, 2H), 7.40 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927715B2
Source datasetuspto-grants-2015_01
ORD IDord-9d32522ba3ee4ce6b67f3a53f683f035
Source noteuspto-grants-2015_01