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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686044Generated: November 2, 2026

Sodium Bicarbonate → HCID 11551838, compound

https://huagongshe.com/reaction/1686044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11551837HCID 11551837—
ProductHCID 11551838HCID 1155183896.4%

Reaction Steps

The compound (20 mg, 0.056 mmol) prepared in Example 81 was treated with a saturated sodium bicarbonate solution to obtain 3-allyl-2-methyl-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1H-pyrrolo[3,2-c]pyridine (14 mg, 0.054 mmol). Sodium hydride (60%, 4.3 mg, 0.108 mmol) was added at room temperature to a solution of 3-allyl-2-methyl-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1H-pyrrolo[3,2-c]pyridine (14 mg, 0.054 mmol) in N,N-dimethylformamide (1 ml) and then the reaction mixture was stirred for 30 minutes. Iodomethane (0.004 ml, 0.06 mmol) was added to the reaction mixture, which was then stirred for 1 hour at room temperature. The reaction mixture was diluted with ethyl acetate (10 ml) and washed with water (10 ml) three times. The organic layer was separated, dried on anhydrous magnesium sulfate, and then concentrated. The resulting residue was dissolved in ethyl acetate (1 ml), saturated with hydrochloric acid gas, and then filtered to give the titled compound as a white solid. (Yield: 42.3%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148529B2
Source datasetuspto-grants-2012_04
ORD IDord-a5eb2de761a54122a24da60b4f940f04
Source noteuspto-grants-2012_04