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30235-26-8

30235-26-8 Structure

30235-26-8 Structure
IdentificationBack Directory
[Name]

4-PYRIDIN-2-YL-THIAZOL-2-YLAMINE
[CAS]

30235-26-8
[Synonyms]

BUTTPARK 29\06-84
TIMTEC-BB SBB010613
IFLAB-BB F0447-0233
4-(2-pyridyl)-2-thiazolamine
4-(2-pyridyl)thiazol-2-amine
2-AMINO-4-(2-PYRIDYL)THIAZOLE
4-(2-Pyridinyl)-2-thiazolamine
4-(2-Pyridinyl)thiazol-2-amine
4-(Pyridin-2-yl)thiazol-2-amine
4-PYRIDIN-2-YL-THIAZOL-2-YLAMINE
[4-(2-pyridyl)thiazol-2-yl]amine
2-ThiazolaMine, 4-(2-pyridinyl)-
2-Amino-4-(2-pyridyl)thiazole,97%
4-PYRIDIN-2-YL-1,3-THIAZOL-2-AMINE
4-(2-PYRIDINYL)-1,3-THIAZOL-2-AMINE
4-(2-pyridinyl)-1,3-thiazol-2-amine(SALTDATA: FREE)
4-PYRIDIN-2-YL-THIAZOL-2-YLAMINE ISO 9001:2015 REACH
[Molecular Formula]

C8H7N3S
[MDL Number]

MFCD00460417
[MOL File]

30235-26-8.mol
[Molecular Weight]

177.23
Chemical PropertiesBack Directory
[Melting point ]

173-174 °C(Solv: ethanol, 50% (64-17-5))
[Boiling point ]

383.6±17.0 °C(Predicted)
[density ]

1.333±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[form ]

Solid
[pka]

3.40±0.10(Predicted)
[color ]

Pale brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HazardClass ]

IRRITANT
[HS Code ]

2934100090
Spectrum DetailBack Directory
[Spectrum Detail]

4-PYRIDIN-2-YL-THIAZOL-2-YLAMINE(30235-26-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-bromo-1-pyridin-2-yl-ethanone

40086-66-6

Carbamimidothioic acid

17356-08-0

4-PYRIDIN-2-YL-THIAZOL-2-YLAMINE

30235-26-8

General procedure for the synthesis of 4-(pyridin-2-yl)thiazol-2-amine from 2-bromo-1-(2-pyridinyl)ethanone and thiourea (CAS: 17356-08-0): 2-bromo-1-(2-pyridinyl)ethanone (0.01 mol, ca. 0.76 g), thiourea (0.01 mol), and 50 mL of ethanol were added to a 100 mL round-bottomed flask, and the mixture was heated to reflux for for 4 hours. After completion of the reaction, the ethanol solvent was removed by distillation under reduced pressure. The crude product was purified by column chromatography using dichloromethane (DCM): methanol (MeOH): ammonium hydroxide (NH4OH) (20:1:0.1, v/v) as mobile phase. 4-(Pyridin-2-yl)thiazol-2-amine was finally obtained as a white solid in a yield of 1.41 g in 79.6%.

[References]

[1] Patent: CN105820163, 2016, A. Location in patent: Paragraph 0127 - 0129
[2] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 2, p. 560 - 564
[3] Patent: WO2008/122787, 2008, A1. Location in patent: Page/Page column 85
[4] Journal of Heterocyclic Chemistry, 1970, vol. 7, p. 1137 - 1141
[5] Journal of the Chinese Chemical Society, 2017, vol. 64, # 12, p. 1408 - 1416
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