1078151-34-4

Basic information

• Product Name: 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid
• Synonyms: 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid;Thieno[3,2-c]pyridine-5(4H)-carboxylic acid, 2-borono-6,7-dihydro-, 5-(1,1-diMethylethyl) ester;(5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl)boronic acid
• CAS NO: 1078151-34-4
• Molecular Formula: C₁₂H₁₈BNO₄S
• Molecular Weight: 285.1675
• Mol File: 1078151-34-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 474.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.29±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 8.60±0.20(Predicted)
• CAS DataBase Reference: 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid(1078151-34-4)
• EPA Substance Registry System: 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid(1078151-34-4)

Safety Data

• Hazardous Substances Data: 1078151-34-4(Hazardous Substances Data)

Usage

General Description

5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid is a chemical compound made up of a thienopyridine core structure with a boronic acid functional group and a tert-butoxycarbonyl protecting group. 5-(tert-butoxycarbonyl)-3a,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridin-2-ylboronic acid is often used in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It has potential applications in medicinal chemistry for the development of new drugs and pharmaceuticals. Additionally, its boronic acid moiety gives it the ability to participate in Suzuki-Miyaura coupling reactions, making it a valuable tool in the synthesis of complex organic molecules.

Upstream product

• 230301-73-2 6,7-dihydro-4H-thieno[3,2-c]-pyridine-5-carboxylic acid tert-butyl ester 

Downstream Products

• 1142947-94-1 tert-butyl 2-(2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate 
• 1142947-31-6 2-{2-[4-(2-methyl-imidazol-1-ylmethyl)-phenylamino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}-6,7-dihydro-4H-thieno[3,2-c]pyridine-5-carboxylic acid tert-butyl ester 
• 1142946-99-3 tert-butyl 2-(2-{[3-(4-methylpiperazin-1-yl)phenyl]amino}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate 
• 1142947-11-2 tert-butyl 2-(2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate 

Relevant articles and documents

PYRROLOPYRIMIDINE COMPOUNDS AND THEIR USE AS JANUS KINASE MODULATORS

Provided herein are pyrrolopyrimidine compounds of Formula (I) wherein R1 is a heteroaryl containing at least one S atom, and optionally substituted on a ring carbon by one, two, or three substituents each independently selected from the group consisting of : halo, hydroxyl, nitro, formyl, formamido, cyano, sulfonyl, carboxy, amino, amido, acylamino, carbamoyl, sulphamoyl, alkyl, alkenyl, CF3, ureido, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, carbaldehyde oxime, N -alkylsulphamoyl, N-alkylcarbamoyl, -OR13R11 or -R13R11; R2 is phenyl or pyridinyl, wherein R2 optionally substituted on a ring carbon by one, two, or three substituents each indenpendently selected from the group consisting of : halo, hydroxyl, cyano, nitro, formyl, formamido, carboxy, sulfonyl, amino, amido, -N- alkyl -amino, carbamoyl, sulphamoyl, CF3, ureido, alkyl, alkenyl, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, N-alkylsulphamoyl, N-alkylcarbamoyl, -OR11, -OR12R11, or -R12R11; and methods of making and using the same. Such compounds may be used in inflammatory or myeloproliferative disorders. The disclosure also provides for treating cancer.