HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577481Generated: October 28, 2026
Sodium hydride → 2-{[2-(benzyloxy)-4,6-dimethylpyridin-3-yl]methyl}-8-iodo-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one
https://huagongshe.com/reaction/577481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Benzyloxy)-3-(chloromethyl)-4,6-dimethylpyridine | HCID 61257868 | — |
| Reactant | 8-iodo-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 86723706 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-{[2-(benzyloxy)-4,6-dimethylpyridin-3-yl]methyl}-8-iodo-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one | HCID 86723707 | 91% |
Reaction Steps
To a solution of 8-iodo-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (53b, 2.08 mg, 5.22 mmol) in anhydrous DMF (30 mL) was added NaH (420 mg, 10.4 mmol, 60% in oil) at 0° C. under N2 atmosphere for 30 minutes. 2-(benzyloxy)-3-(chloromethyl)-4,6-dimethylpyridine (Cpd Z, 1.89 g, 7.83 mmol) was added to the mixture. The resulting mixture was stirred at room temperature for 14 hours. The mixture was quenched with H2O (60 mL) and extracted with EtOAc (4×80 mL). The combined organic layers were washed with brine (2×50 mL), dried over Na2SO4 and concentrated under vacuum. The residue was purified by prep.HPLC to give 2-{[2-(benzyloxy)-4,6-dimethylpyridin-3-yl]methyl}-8-iodo-7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (53c, 2.5 g, 91%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040515B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-39a6e8716eb04608b920a19630b06271 |
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| Source note | uspto-grants-2015_05 |
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