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5-Bromopyrimidin-4-amine

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5-Bromopyrimidin-4-amine Basic information
Product Name:5-Bromopyrimidin-4-amine
Synonyms:4-AMINO-5-BROMOPYRIMIDINE;Pyrimidine, 4-amino-5-bromo-;4-Pyrimidinamine, 5-bromo-;4-Amino-5-bromopyrimidine,98%;5-BROMOPYRIMIDIN-4-AMINE ISO 9001:2015 REACH;5-Bromopyrimidin-4-amine
CAS:1439-10-7
MF:C4H4BrN3
MW:174
EINECS:
Product Categories:Heterocycle-Pyrimidine series;Pyrimidine series
Mol File:1439-10-7.mol
5-Bromopyrimidin-4-amine Structure
5-Bromopyrimidin-4-amine Chemical Properties
Melting point 207-211℃
Boiling point 282.2±20.0 °C(Predicted)
density 1.844±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form Powder
pka3+-.0.10(Predicted)
color Pale brown
Water Solubility Slightly soluble in water.
InChIInChI=1S/C4H4BrN3/c5-3-1-7-2-8-4(3)6/h1-2H,(H2,6,7,8)
InChIKeyIIFAONYUCDAVGA-UHFFFAOYSA-N
SMILESC1=NC=C(Br)C(N)=N1
Safety Information
HS Code 2933599590
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
5-Bromopyrimidin-4-amine Usage And Synthesis
UsesIt is an inhibitor of thymidine phosphorylase, an enzyme known to be over-expressed in several tumor types and to play a role in metastasis.
Synthesis
4(1H)-Pyrimidinimine (9CI)

163133-86-6

5-BROMOPYRIMIDIN-4-AMINE

1439-10-7

The synthesis of 4-amino-5-bromopyrimidine was carried out using the compound (CAS: 163133-86-6) as starting material according to a modified scheme of the literature method 7: 4-aminopyrimidine (1.00 g, 10.5 mmol, 1.0 eq.) was dissolved in water (20 mL) with CaCO3 (263 mg, 2.63 mmol, 0.25 eq.) followed by slow addition of bromine (Br2, 1.06 mL, 20.5 mmol, 2.0 eq.). The reaction mixture was stirred at 60 °C for 45 min, then cooled to room temperature and poured into dichloromethane (CH2Cl2, 20 mL) for layering. After separation of the organic layer, the aqueous layer was further extracted with dichloromethane (2 x 20 mL). All organic layers were combined and stored temporarily. The aqueous layer was adjusted to pH 9-10 with 20% aqueous K2CO3 to induce precipitation of the product. The precipitate was collected by filtration and dried to afford the target product 4-amino-5-bromopyrimidine (1.08 g, 6.22 mmol, 59% yield) as a light tan solid.

References[1] Journal of Organic Chemistry, 1983, vol. 48, # 7, p. 1064 - 1069
[2] Chemical and Pharmaceutical Bulletin, 1993, vol. 41, # 1, p. 81 - 86
[3] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 12, p. 3654 - 3661
[4] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 21, p. 5247 - 5250
[5] European Journal of Medicinal Chemistry, 2008, vol. 43, # 6, p. 1248 - 1260
5-Bromopyrimidin-4-amine Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Ethyl acetate-->Diethyl ether-->Acetic acid-->Petroleum ether-->Bromine-->Sodium bicarbonate-->Palladium hydroxide-->4-Aminopyrimidine-->4-Amino-2,6-dichloropyrimidine
Preparation Products9H-Pyrimido[4,5-b]indole
Tag:5-Bromopyrimidin-4-amine(1439-10-7) Related Product Information
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