2-Thiazolamine, 5-(1-methylethyl)-

2-Thiazolamine, 5-(1-methylethyl)- Suppliers list
Company Name: Chengdu Kamel Pharmaceutical Co., Ltd  Gold
Tel: 028-67136579 15828051124
Email: sales@kamelpharm.com
Company Name: Wuhan Kaymke Chemical Co., Ltd.,  Gold
Tel: 027-87342388 18086026008
Email: sales@kaymke.com
Company Name: Wuhan Co TC SR Technology Co., Ltd.  Gold
Tel: 027-13487090-306 13487090306
Email: 48011371@qq.com
Company Name: Nanjing Chengqian Pharmaceutical Technology Co., Ltd.  Gold
Tel: 025-52791040 18652036685
Email: haozhongwen@126.com
Company Name: Beijing InnoChem Science & Technology Co., Ltd.  Gold
Tel: 15652467323
Email: sales@inno-chem.com.cn
2-Thiazolamine, 5-(1-methylethyl)- Basic information
Product Name:2-Thiazolamine, 5-(1-methylethyl)-
Synonyms:2-Thiazolamine, 5-(1-methylethyl)-;2-Amino-5-isopropy-thiazole;2-Amino-5-isopropylthiazole;5-isopropyl-1,3-thiazol-2-amine;5-Isopropylthiazol-2-aMine;5-Isopropyl-thiazol-2-ylaMine;5-(propan-2-yl)-1,3-thiazol-2-amine
CAS:101080-15-3
MF:C6H10N2S
MW:142.22
EINECS:
Product Categories:
Mol File:101080-15-3.mol
2-Thiazolamine,  5-(1-methylethyl)- Structure
2-Thiazolamine, 5-(1-methylethyl)- Chemical Properties
Boiling point 110-115 °C(Press: 5 Torr)
density 1.142±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka5.32±0.10(Predicted)
AppearanceLight yellow to yellow Liquid
InChIInChI=1S/C6H10N2S/c1-4(2)5-3-8-6(7)9-5/h3-4H,1-2H3,(H2,7,8)
InChIKeyMENMPXBUKLPJKR-UHFFFAOYSA-N
SMILESS1C(C(C)C)=CN=C1N
Safety Information
MSDS Information
2-Thiazolamine, 5-(1-methylethyl)- Usage And Synthesis
Synthesis
Butanal, 2-bromo-3-methyl-

64932-36-1

Carbamimidothioic acid

17356-08-0

2-Thiazolamine,  5-(1-methylethyl)-

101080-15-3

General procedure: To a dichloromethane/dioxane (V/V = 4/1) solution of isovaleraldehyde (1.721 g, 20 mmol) was slowly added dropwise a dichloromethane/dioxane (V/V = 4/1) solution of bromine (1.0 mL, 20 mmol). The reaction mixture was stirred at 10 °C to give 2-bromoisovaleraldehyde intermediate. Subsequently, 2-bromoisovaleraldehyde intermediate was slowly added dropwise to a dichloromethane/dioxane (30 mL) solution of thiourea (1.523 g, 20 mmol). Ethanol (6 mL) and triethylamine (2.424 g, 24 mmol) were added and the reaction was carried out at room temperature for 20 hours. Upon completion of the reaction, 100 mL of distilled water was added to the reaction mixture and the pH was adjusted to 12 with 12 N sodium hydroxide solution. after continued stirring for 1 h at room temperature, extraction was carried out with dichloromethane and water. The organic layer was washed with saturated brine and dried with anhydrous magnesium sulfate. Finally, the target compound 5-isopropylthiazol-2-amine was purified by silica gel column chromatography to give the target compound 5-isopropylthiazol-2-amine (1.202 g, 42.26% yield).

References[1] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 22, p. 5521 - 5525
[2] European Journal of Medicinal Chemistry, 1999, vol. 34, # 10, p. 883 - 889
[3] Patent: WO2005/95367, 2005, A1. Location in patent: Page/Page column 28
[4] Journal of Medicinal Chemistry, 2011, vol. 54, # 12, p. 4119 - 4132
2-Thiazolamine, 5-(1-methylethyl)- Preparation Products And Raw materials
Raw materialsButanal, 2-bromo-3-methyl--->4-methylvaleraldehyde-->Carbamimidothioic acid-->3-Methyl-1-butanol-->Ammonia-->1,4-Dioxane-->Dichloromethane-->Isovaleraldehyde-->Triethylamine-->Ethanol
Tag:2-Thiazolamine, 5-(1-methylethyl)-(101080-15-3) Related Product Information