HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633976Generated: October 25, 2026
Triethylamine → 5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amine
https://huagongshe.com/reaction/633976
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylpiperazine-1-ethylamine | HCID 70284 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Amino-5-bromonicotinaldehyde hydrobromide | HCID 86606146 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amine | HCID 67154522 | — |
Reaction Steps
Triethylamine (1.0 mL, 7.09 mmol) was added to a solution of 2-amino-5-bromonicotinaldehyde hydrobromide (1.0 g, 3.54 mmol) in methanol (24 mL) at room temperature. The reaction mixture was stirred for 10 minutes prior to the addition of 2-(4-methylpiperazin-1-yl)ethanamine (558 mg, 3.90 mmol). The reaction mixture was then stirred overnight and cooled to 0° C. Sodium borohydride (201 mg, 5.32 mmol) was added portionwise at 0° C. and the reaction mixture was allowed to reach room temperature and stirred for 4 hours. After concentration to dryness, the residue was purified by chromatography on silica gel using dichloromethane/methanol/ammoniac (10:0:0.1 to 9:1:0.1) as eluent. The title product was obtained as a yellow solid (560 mg, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321769B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-42bfe850ccd542f5893df646b6f5d588 |
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| Source note | uspto-grants-2016_04 |
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