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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
Molecular Weight:
174
MDL Number:
MFCD09999203
MOL File:
849353-34-0.mol
MSDS File:
SDS
Last updated:2026-09-12 18:48:00

5-Amino-4-bromopyrimidine Properties

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

SAFETY

Risk and Safety Statements

HS Code  2933599590

5-Amino-4-bromopyrimidine price More Price(40)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR927026 5-Amino-4-bromopyrimidine 95% 849353-34-0 250mg $88 2026-06-04 Buy
Apolloscientific OR927026 5-Amino-4-bromopyrimidine 95% 849353-34-0 1g $181 2026-06-04 Buy
Activate Scientific AS30879 5-Amino-4-bromopyrimidine 98% 849353-34-0 1g $224 2026-06-04 Buy
Activate Scientific AS30879 5-Amino-4-bromopyrimidine 98% 849353-34-0 5g $726 2026-06-04 Buy
aablocks AA0052Y3 4-Bromo-5-pyrimidinamine 95% 849353-34-0 250mg $62 2026-05-28 Buy
Product number Packaging Price Buy
OR927026 250mg $88 Buy
OR927026 1g $181 Buy
AS30879 1g $224 Buy
AS30879 5g $726 Buy
AA0052Y3 250mg $62 Buy

5-Amino-4-bromopyrimidine Chemical Properties, Uses, Production

Uses

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

Synthesis

5-AMINOPYRIMIDINE

591-55-9

5-AMINO-4-BROMOPYRIMIDINE

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

Global Suppliers ( 66)
Supplier Tel Email Country ProdList Advantage
PharmaBlock Sciences (Nanjing),Inc. 025-86918202 4000255188 sales@pharmablock.com China 5000 55
Pure Chemistry Scientific Inc. 001-857-928-2050 or 1-888-588-9418 sales@chemreagents.com United States 10174 62
Tetranov Biopharm 13526569071 sales@leadmedpharm.com China 7880 64
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57
Shanghai Sunway Pharmaceutical Technology Co., Ltd 13761987713 hxzheng@sunwaypharm.cn China 8663 57
Shanghai Hekang Biotechnology Co., Ltd. 17721021104 18939837085 2880152141@qq.com China 1840 55
Bide Pharmatech Ltd. 400-164-7117 18317119277 product02@bidepharm.com China 40000 60
Shanghai Worldyang Chemical Co.,Ltd. 021-56795766 sales@worldyachem.com China 9475 58
Hangzhou Milestone Pharmtech Co., Ltd. 0571-82896630 18969958410 sales_hz@milestonepharmtech.com China 4909 55

View Latest Price from 5-Amino-4-bromopyrimidine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
5-AMINO-4-BROMOPYRIMIDINE  pictures 2026-08-20 5-AMINO-4-BROMOPYRIMIDINE
849353-34-0
$1.10 1g 99.00% 100 Tons Min Dideu Industries Group Limited
5-AMINO-4-BROMOPYRIMIDINE pictures 2019-12-26 5-AMINO-4-BROMOPYRIMIDINE
849353-34-0
1KG 95%-99% 1kg; 100kg; 1000kg Career Henan Chemical Co
4-bromopyrimidin-5-ylamine 5-Pyrimidinamine, 4-bromo- 5-AMINO-4-BROMOPYRIMIDINE ISO 9001:2015 REACH 5-Amino-4-bromopyrimidine 849353-34-0 Heterocycle-Pyrimidine series