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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932364Generated: November 1, 2026

Sodium Bicarbonate → HCID 67141929, compound

https://huagongshe.com/reaction/1932364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67141928HCID 67141928—
ProductHCID 67141929HCID 67141929—

Reaction Steps

The compound prepared in Example 613 was treated with a saturated sodium bicarbonate solution to obtain 2-[1-(3-fluorobenzyl)-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl]-1,2,3,4-tetrahydroisoquinoline. Morpholine (25 μl, 0.297 mmol), acetic acid (0.13 ml), and formaldehyde (70 μl) were added to a solution of 2-[1-(3-fluorobenzyl)-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl]-1,2,3,4-tetrahydroisoquinoline (100 mg, 0.27 mmol) in ethanol (1.5 ml). The reaction mixture was refluxed overnight and then concentrated under reduced pressure. The resulting residue was dissolved in ethyl acetate and then washed with a sodium bicarbonate solution. The organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/dichloromethane=1/1, v/v) to give the titled compound as a pale yellow solid (Yield: 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188114B2
Source datasetuspto-grants-2012_05
ORD IDord-afad65c5d34241128b176f76ff8521a2
Source noteuspto-grants-2012_05