| Identification | Back Directory | [Name]
4-BROMOPYRIDINE-2-CARBALDEHYDE | [CAS]
131747-63-2 | [Synonyms]
4-BROMOPICOLINALDEHYDE
4-Bromopyridine-2-carbaL
4-broMopyridin-2-carbaldehyde
4-BROMO-2-PYRIDINECARBALDEHYDE
4-BROMOPYRIDINE-2-CARBALDEHYDE
4-broMo-2-pyridinecarboxaldehyde
2-Pyridinecarboxaldehyde,4-broMo
4-Bromopyridine 2-carboxaldehyde
4-BROMOPYRIDINE-2-CARBALDEHYDE ISO 9001：2015 REACH | [EINECS(EC#)]
606-385-7 | [Molecular Formula]
C6H4BrNO | [MDL Number]
MFCD08690697 | [MOL File]
131747-63-2.mol | [Molecular Weight]
186.01 |
| Chemical Properties | Back Directory | [Boiling point ]
244.0±20.0 °C(Predicted) | [density ]
1.683±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [solubility ]
Chloroform (Slightly), DMSO (Sparingly) | [form ]
solid | [pka]
1.78±0.10(Predicted) | [color ]
Off-white to light yellow |
| Hazard Information | Back Directory | [Uses]
4-Bromopyridine-2-carboxaldehyde is a reagent used to synthesize Curcumin (C838500) analogues. It can also be used to prepare 1,4-dihydropyridine calcium antagonists. | [Synthesis]
General procedure for the synthesis of 4-bromopyridine-2-carboxaldehyde from 2-hydroxymethyl-4-bromopyridine: 3L of dichloromethane (DCM) was added to a 5L three-necked flask under nitrogen protection, and cooled to -60 °C. During the cooling process, 240 g of oxalyl chloride was added slowly and dropwise. Maintaining the reaction temperature at -60 °C, 295.6 g of dimethyl sulfoxide (DMSO) was added dropwise to the reaction system and held for 30 min after the dropwise addition. Subsequently, 237.5 g of 2-hydroxymethyl-4-bromopyridine (Cpd 3) was slowly added dropwise at -60 °C and the reaction was continued at -65 °C for 1 hour. At this temperature, 3.5 equivalents of triethylamine (TEA) was added, and the reaction solution was allowed to stand before the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the target product 4-bromopyridine-2-carboxaldehyde (Compound 4) was purified by column chromatography to give 177.2 g in 75% yield. | [References]
[1] Patent: US2010/125082, 2010, A1. Location in patent: Page/Page column 24
[2] Tetrahedron, 1997, vol. 53, # 24, p. 8257 - 8268
[3] Patent: CN108516953, 2018, A. Location in patent: Paragraph 0067-0068; 0074-0075; 0076-0083
[4] Chemical and Pharmaceutical Bulletin, 1990, vol. 38, # 9, p. 2446 - 2458
[5] MedChemComm, 2015, vol. 6, # 7, p. 1252 - 1259 |
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