1093075-03-6

Basic information

• Product Name: 5-Chloro-7-(morpholin-4-yl)thiazolo[5,4-d]pyrimidine-2-carboxaldehyde
• Synonyms: 5-Chloro-7-(morpholin-4-yl)thiazolo[5,4-d]pyrimidine-2-carboxaldehyde;5-chloro-7-morpholinothiazolo[5,4-d]pyrimidine-2-carbaldehyde
• CAS NO: 1093075-03-6
• Molecular Formula: C10H9ClN4O2S
• Molecular Weight: 284.726
• Mol File: 1093075-03-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-Chloro-7-(morpholin-4-yl)thiazolo[5,4-d]pyrimidine-2-carboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Chloro-7-(morpholin-4-yl)thiazolo[5,4-d]pyrimidine-2-carboxaldehyde(1093075-03-6)
• EPA Substance Registry System: 5-Chloro-7-(morpholin-4-yl)thiazolo[5,4-d]pyrimidine-2-carboxaldehyde(1093075-03-6)

Safety Data

• Hazardous Substances Data: 1093075-03-6(Hazardous Substances Data)

Upstream product

• 31785-05-4 5-amino-2-methyl-1,3-thiazole-4-carboxylic acid ethyl ester 
• 90877-70-6 ethyl 2-acetamido-2-cyanoacetate 
• 1093075-02-5 2-(5-chloro-7-morpholin-4-yl-thiazolo[5,4-d]pyrimidin-2-yl)-1-phenyl-ethanol 
• 1093074-92-0 5-chloro-2-methyl-7-morpholin-4-yl-thiazolo[5,4-d]pyrimidine 
• 1093074-91-9 2-methyl-5-ureido-thiazole-4-carboxylic acid ethyl ester 
• 7464-11-1 5,7-dichloro-2-methyl-thiazolo[5,4-d]pyrimidine 
• 5021-52-3 2-methyl-4H-thiazolo[5,4-d]pyrimidine-5,7-dione 
• 41975-14-8 5-chloro-7-morpholin-4-yl-thiazolo[5,4-d]pyrimidine 
• 68-12-2 N,N-dimethyl-formamide 
• 1093075-04-7 5-chloro-7-morpholin-4-yl-2-styryl-thiazolo[5,4-d]pyrimidine 
• 13479-88-4 5,7-dichloro-[1,3]thiazolo[5,4-d]pyrimidine 

Downstream Products

• 1257294-60-2 C₁₈H₂₆ClN₅O₂S 

Relevant articles and documents

Potent and highly selective benzimidazole inhibitors of PI3-kinase delta

Inhibition of PI3Kδ is considered to be an attractive mechanism for the treatment of inflammatory diseases and leukocyte malignancies. Using a structure-based design approach, we have identified a series of potent and selective benzimidazole-based inhibitors of PI3Kδ. These inhibitors do not occupy the selectivity pocket between Trp760 and Met752 that is induced by other families of PI3Kδ inhibitors. Instead, the selectivity of the compounds for inhibition of PI3Kδ relative to other PI3K isoforms appears to be due primarily to the strong interactions these inhibitors are able to make with Trp760 in the PI3Kδ binding pocket. The pharmacokinetic properties and the ability of compound 5 to inhibit the function of B-cells in vivo are described.

THIAZOLIOPYRIMIDINES AND THEIR USE AS INHIBITORS OF PHOSPHATIDYLINOSITOL-3 KINASE

Thiazolopyrimidines of formula (I): wherein W represents a thiazole ring; R1 and R2 form, together with the N atom to which they are attached, a group of the following formula (IIa): in which A is a ring system; m is 0, 1 or 2; Rsup