Pyrimidine, 5-bromo-2-ethyl- (9CI)
Pyrimidine, 5-bromo-2-ethyl- (9CI) Basic information
- Product Name:
- Pyrimidine, 5-bromo-2-ethyl- (9CI)
- Synonyms:
-
- PyriMidine, 5-broMo-2-ethyl-
- Pyrimidine, 5-bromo-2-ethyl- (9CI)
- 5-Bromo-2-ethylpyrimidine
- 5-Bromo-2-ethyl-pyrimidin
- Pyrimidine, 5-bromo-2-ethyl- (9CI) ISO 9001:2015 REACH
- CAS:
- 873331-73-8
- MF:
- C6H7BrN2
- MW:
- 187.04
- Product Categories:
-
- Heterocycle-Pyrimidine series
- PYRIMIDINE
- Mol File:
- 873331-73-8.mol
Pyrimidine, 5-bromo-2-ethyl- (9CI) Chemical Properties
- Boiling point:
- 211.8±13.0 °C(Predicted)
- Density
- 1.497±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 0.56±0.22(Predicted)
- InChI
- InChI=1S/C6H7BrN2/c1-2-6-8-3-5(7)4-9-6/h3-4H,2H2,1H3
- InChIKey
- SQOJDBHJUUGQJP-UHFFFAOYSA-N
- SMILES
- C1(CC)=NC=C(Br)C=N1
Pyrimidine, 5-bromo-2-ethyl- (9CI) Usage And Synthesis
Synthesis
1235450-86-8
873331-73-8
General procedure for the synthesis of 5-bromo-2-ethylpyrimidine from 5-bromo-2-ethyl-4-pyrimidinecarboxylic acid: 5-bromo-2-ethyl-4-pyrimidinecarboxylic acid (5.6 g, 24.3 mmol) was dissolved in xylene (50 mL), and the reaction was carried out at reflux for 2 hours. After completion of the reaction, the reaction mixture was cooled and the sample was directly upsampled onto a silica gel column, eluting first with petroleum ether and then with petroleum ether solution containing 5% ethyl acetate, and the target fractions were collected to afford compound 0601-121 (1.7 g, 38% yield) as a yellow liquid.1H NMR (400 MHz, DMSO-d6) δ: 1.26 (t, J = 7.6 Hz, 3H) 2.87 (q, J = 7.6 Hz, 2H), 8.90 (s, 2H).
References
[1] Patent: WO2011/130628, 2011, A1. Location in patent: Page/Page column 178
[2] Patent: US2013/102595, 2013, A1. Location in patent: Paragraph 0373
[3] Patent: JP2015/187145, 2015, A. Location in patent: Paragraph 0326
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