(2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL
(2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL Basic information
- Product Name:
- (2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL
- Synonyms:
-
- RARECHEM AL BD 1354
- 2,4-DIMETHYLTHIAZOLE-5-METHANOL
- (2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL
- (2,4-Dimethylthiazol-5-yl)methanol
- 2,4-Dimethyl-5-(hydroxymethyl)-1,3-thiazole
- (2,4-dimethyl-5-thiazolyl)methanol
- 5-Thiazolemethanol, 2,4-dimethyl-
- 2,4-Dimethyl-5-thiazolemethanol
- CAS:
- 50382-32-6
- MF:
- C6H9NOS
- MW:
- 143.21
- Mol File:
- 50382-32-6.mol
(2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL Chemical Properties
- Melting point:
- 56 °C
- Boiling point:
- 111-119°C 1mm
- Density
- 1.208±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 13.66±0.10(Predicted)
- Appearance
- Light yellow to yellow Solid
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-41
- Safety Statements
- 26-37/39-39
- Hazard Note
- Irritant
- HS Code
- 2934100090
(2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL Usage And Synthesis
Synthesis
7210-77-7
50382-32-6
General procedure for the synthesis of (2,4-dimethyl-1,3-thiazol-5-yl)methanol from ethyl 2,4-dimethylthiazole-5-carboxylate: ethyl 2,4-dimethylthiazole-5-carboxylate (500 mg, 2.70 mmol) was dissolved in anhydrous tetrahydrofuran (10 mL), and lithium aluminium hydroxide (205 mg, 5.40 mmol) was slowly added at 0 °C. After the reaction lasted for 1 h, the reaction was quenched by careful addition of water (10 mL). Subsequently, the reaction mixture was extracted with ethyl acetate (15 mL x 3), the organic phases were combined and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the reaction was purified by preparative thin layer chromatography (TLC) plates (unfolding reagent ratio 1:1 petroleum ether/ethyl acetate, Rf = 0.4) to afford the target product (2,4-dimethyl-1,3-thiazol-5-yl)methanol (300 mg, yellow solid) in 77% yield.1H NMR (400 MHz, methanol-d4) δ: 4.68 (s, 2H) 2.64 (s, 3H), 2.33 (s, 3H).
References
[1] Patent: EP3299371, 2018, A1. Location in patent: Paragraph 0252; 0253; 0254
[2] Journal of Medicinal Chemistry, 1973, vol. 16, p. 978 - 984
[3] Patent: EP1186604, 2002, A1. Location in patent: Page 131-132
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(2,4-DIMETHYL-1,3-THIAZOL-5-YL)METHANOL(50382-32-6)Related Product Information
- 4-METHYL-2-(3-PYRIDINYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID
- 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
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- 4-METHYL-2-[4-(TRIFLUOROMETHYL)PHENYL]THIAZOLE-5-CARBOXYLIC ACID
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- ETHYL 4-(TRIFLUOROMETHYL)-2-METHYLTHIAZOLE-5-CARBOXYLATE
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- 2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLIC ACID
- ETHYL 4-METHYL-2-[3-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOLE-5-CARBOXYLATE
- 2-OXO-2-PHENYLETHYL 2-METHYL-4-(TRIFLUOROMETHYL)-1,3-THIAZOLE-5-CARBOXYLATE