Uses
ChemicalBook > CAS DataBase List > 5-AMINO-4-BROMOPYRIMIDINE

5-AMINO-4-BROMOPYRIMIDINE

Uses
Product Name
5-AMINO-4-BROMOPYRIMIDINE
CAS No.
849353-34-0
Chemical Name
5-AMINO-4-BROMOPYRIMIDINE
Synonyms
5-AMINO-4-BROMOPYRIMIDINE;5-Pyrimidinamine, 4-bromo-;4-bromopyrimidin-5-ylamine;5-AMINO-4-BROMOPYRIMIDINE ISO 9001:2015 REACH
CBNumber
CB02453754
Molecular Formula
C4H4BrN3
Formula Weight
174
MOL File
849353-34-0.mol
More
Less

5-AMINO-4-BROMOPYRIMIDINE Property

Boiling point:
282.2±20.0 °C(Predicted)
Density 
1.844±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
pka
1.10±0.16(Predicted)
Appearance
Light yellow to yellow Solid
InChI
InChI=1S/C4H4BrN3/c5-4-3(6)1-7-2-8-4/h1-2H,6H2
InChIKey
NXYSMLJPDPVHOE-UHFFFAOYSA-N
SMILES
C1=NC=C(N)C(Br)=N1
More
Less

Safety

HS Code 
2933599590
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FB139430
Product name
4-Bromopyrimidin-5-amine
Packaging
50mg
Price
$80
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB139430
Product name
4-Bromopyrimidin-5-amine
Packaging
100mg
Price
$125
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB139430
Product name
4-Bromopyrimidin-5-amine
Packaging
250mg
Price
$200
Updated
2021/12/16
AK Scientific
Product number
W8767
Product name
5-Amino-4-bromopyrimidine
Packaging
1g
Price
$251
Updated
2021/12/16
Matrix Scientific
Product number
072459
Product name
5-Amino-4-bromopyrimidine
Purity
95+%
Packaging
500mg
Price
$265
Updated
2021/12/16
More
Less

5-AMINO-4-BROMOPYRIMIDINE Chemical Properties,Usage,Production

Uses

5-Amino-4-bromopyrimidine is a useful research chemical compound.

Synthesis

591-55-9

849353-34-0

General procedure for the synthesis of 5-amino-4-bromopyrimidine from 5-aminopyrimidine: 1. 5-amino-4,6-dichloropyridine (5.0 g, 30.5 mmol) was dissolved in 250 mL of diethyl ether, to which was added sodium hydroxide solution (20.0 g, 0.50 mol, dissolved in 60 mL of water) and palladium catalyst (10% carbon-loaded palladium, 400 mg). 2. The mixture was placed in a Parr shaker and the reaction was shaken at room temperature under 50 psi hydrogen pressure for 20 hours. 3. Upon completion of the reaction, the mixture was filtered through a CELITES filter aid to separate the organic and aqueous phases. The aqueous phase was extracted with three 100mL portions of ethyl acetate. 4. The organic layers were combined, dried with magnesium sulfate, filtered and concentrated in vacuum. The crude product was crystallized from ethyl acetate to give pyrimidin-5-ylamine as a white crystalline solid (2.8 g, 95% yield). 5. The bromination of pyrimidin-5-ylamine was carried out under the same conditions as for the preparation of 4-amino-3-bromo-2,6-dimethylpyridine. The crude product (300 mg, 35% yield) obtained was of sufficient purity to be used without further purification. Alternative synthetic method: 1. 4,6-Dichloro-5-aminopyrimidine (21 g, 128 mmol) was dissolved in 250 mL of methanol and ammonium formate (45 g, 714 mmol) and palladium catalyst (10% carbon-loaded palladium, 1 g, 0.943 mmol) were added sequentially at 0°C. 2. The mixture was stirred at room temperature overnight and after completion of the reaction was filtered through a CELITEO filter aid. 3. The filtrate was concentrated to give a yellow solid to which 100 mL of water and 250 mL of ethyl acetate were added. The organic phase was separated and the aqueous phase was extracted with eight 250mL of ethyl acetate. 4. The organic layers were combined, dried with magnesium sulfate, filtered and concentrated in vacuum to give off-white crystals (8.1 g, 67%). 5. 5-Aminopyridine (3.0 g, 31.5 mmol) was dissolved in 150 mL of dichloromethane and 30 mL of methanol and cooled to 0°C. Benzyltrimethylammonium tribromide (13.5 g, 34.7 mmol) was added in batches over 10 min. 6. Stirring was continued at 0 °C for 15 min and then at room temperature for 90 min. The reaction mixture was adjusted to pH 8 with aqueous sodium bicarbonate. 7. The organic layer was separated and the aqueous layer was extracted with three 30 mL of ethyl acetate. The organic extracts were combined, dried with sodium sulfate, filtered and concentrated in vacuum to give an off-white solid (2.8 g, 51%) of sufficient purity to be used without further purification.

References

[1] Patent: WO2005/30213, 2005, A1. Location in patent: Page/Page column 177
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 4, p. 1583 - 1598
[3] Patent: WO2013/117649, 2013, A1. Location in patent: Paragraph 0053

5-AMINO-4-BROMOPYRIMIDINE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

5-AMINO-4-BROMOPYRIMIDINE Suppliers

SHANGHAI FDC-CHEMICAL CO.,LTD
Tel
021-61469567 13482353728
Fax
021-61161605
Email
sales@fdc-chemical.com
Country
China
ProdList
9713
Advantage
58
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Fax
86-025-86918232
Email
sales@pharmablock.com
Country
China
ProdList
5000
Advantage
55
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
Tetranov Biopharm
Tel
13526569071
Email
sales@leadmedpharm.com
Country
China
ProdList
7892
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Fax
021 51613951
Email
mlcheng@sunwaypharm.cn
Country
China
ProdList
8669
Advantage
57
NovoChemy Ltd.
Tel
021-31261262/ 49 (0)17662837245
Fax
(0)21-33250524
Email
sales@novochemy.com
Country
Germany
ProdList
6328
Advantage
58
Shanghai Hekang Biotechnology Co., Ltd.
Tel
18939837085
Fax
2880152141(QQ)
Email
youchemicals@gmail.com
Country
China
ProdList
1839
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
More
Less

View Lastest Price from 5-AMINO-4-BROMOPYRIMIDINE manufacturers

Dideu Industries Group Limited
Product
5-AMINO-4-BROMOPYRIMIDINE 849353-34-0
Price
US $1.10/g
Min. Order
1g
Purity
99.00%
Supply Ability
100 Tons Min
Release date
2021-12-02
Career Henan Chemical Co
Product
5-AMINO-4-BROMOPYRIMIDINE 849353-34-0
Price
US $0.10/KG
Min. Order
1KG
Purity
95%-99%
Supply Ability
1kg; 100kg; 1000kg
Release date
2019-12-25

849353-34-0, 5-AMINO-4-BROMOPYRIMIDINERelated Search:


  • 5-AMINO-4-BROMOPYRIMIDINE
  • 4-bromopyrimidin-5-ylamine
  • 5-Pyrimidinamine, 4-bromo-
  • 5-AMINO-4-BROMOPYRIMIDINE ISO 9001:2015 REACH
  • 849353-34-0
  • Heterocycle-Pyrimidine series