Production Method 1

5177-27-5

96833-41-9

Reaction Conditions

1.1 Solvents: Methanol ;  rt; 2 h, rt

Reference

Preparation of heteroaryl compounds useful in the treatment of cognitive disorders

, World Intellectual Property Organization, , ,

Production Method 2

5177-27-5

96833-41-9

Reaction Conditions

1.1 Solvents: Methanol ;  0 °C → rt; 2 h, rt; 64 h, rt
1.2 Reagents: Acetic acid ;  rt

Reference

Preparation of N-(heteroaryl)-sulfonamide derivatives useful as S100 inhibitors

, World Intellectual Property Organization, , ,

Production Method 3

5177-27-5

96833-41-9

Reaction Conditions

1.1 Solvents: Methanol ;  16 h, reflux

Reference

Preparation of condensed benzo[b]thiazine derivatives useful as cytoprotectants

, World Intellectual Property Organization, , ,

Production Method 4

5177-27-5

96833-41-9

Reaction Conditions

1.1 Solvents: Methanol ;  1.5 h, rt

Reference

Preparation of pyrrolopyridinamine derivatives as Mps1 inhibitors

, World Intellectual Property Organization, , ,

Production Method 5

5177-27-5

96833-41-9

Reaction Conditions

1.1 Solvents: Methanol ;  16 h, reflux

Reference

Preparation of N-substituted 4-aminophenols and corresponding quinone imines as CytC peroxidase inhibitors useful in treatment of neurodegenerative diseases

, World Intellectual Property Organization, , ,

Production Method 6

96833-41-9

Reaction Conditions

Reference

5-Substituted arylpyrimidines as selective modulators of CRF receptors

, World Intellectual Property Organization, , ,

Production Method 7

96833-41-9

Reaction Conditions

Reference

N-pyrazinyl-2-phenyl-3-pyridinesulfonamides and analogs endothelin receptor antagonists

, World Intellectual Property Organization, , ,

Production Method 8

96833-41-9

Reaction Conditions

Reference

Preparation of N-diazinylbenzenesulfonamides as endothelin receptor antagonists

, United Kingdom, , ,

2-Chloro-4-methoxypyrimidin-5-amine Raw materials

• 5-Amino-2,4-dichloropyrimidine

2-Chloro-4-methoxypyrimidin-5-amine Preparation Products

• 2-Chloro-4-methoxypyrimidin-5-amine (96833-41-9)

• 1. Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy?
  Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
• 2. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 3. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 4. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
• 5. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147

• 15846-15-8(4,6-Dimethoxypyrimidin-5-amine)
• 1698159-51-1(2-Chloro-4-(2-methylpropoxy)pyrimidin-5-amine)
• 96833-50-0(5-Pyrimidinamine, 2-chloro-4-(2-propenyloxy)-)
• 1702077-69-7(2-chloro-4-(propan-2-yloxy)pyrimidin-5-amine)
• 444151-94-4(2-chloro-4,6-dimethoxypyrimidin-5-amine)
• 15579-82-5(4-Methoxypyrimidin-5-amine)
• 1794752-81-0(4-METHOXYPYRIMIDIN-5-AMINE HCL)
• 1701598-01-7(2-Chloro-4-(oxetan-3-yloxy)pyrimidin-5-amine)
• 54484-70-7(2-chloro-4-ethoxypyrimidin-5-amine)
• 1695938-91-0(2-(5-amino-2-chloropyrimidin-4-yl)oxyethan-1-ol)