HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894298Generated: November 3, 2026
Sodium Bicarbonate → HCID 11538745, compound
https://huagongshe.com/reaction/1894298
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 11538744 | HCID 11538744 | — |
| Product | HCID 11538745 | HCID 11538745 | 98.2% |
Reaction Steps
The compound (25 mg, 0.055 mmol) prepared in Example 79 was treated with a saturated sodium bicarbonate solution to obtain 3-(3-fluorobenzyl)-2-methyl-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1H-pyrrolo[3,2-c]pyridine (17 mg, 0.054 mmol). Sodium hydride (60%, 4.3 mg, 0.108 mmol) was added at room temperature to a solution of 3-(3-fluorobenzyl)-2-methyl-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1H-pyrrolo[3,2-c]pyridine (17 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 separated organic layer was 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: 51.2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513277B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-0900b17957354b08aca46d015e1a4c74 |
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| Source note | uspto-grants-2013_08 |
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