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9th February 2014 @ 07:59
Osm: OSM-S-131_to_OSM-S-140

OSM-S-139

Original Sources

Synthesis of 6-bromothieno[3,2-d]pyrimidin-4-amine (21-1) (unsuccessful)

Synthesis of 6-bromothieno[3,2-d]pyrimidin-4-amine (JRC 40-1)

Synthesis of 6-bromothieno[3,2-d]pyrimidin-4-amine (JRC 40-2)

Amination of bromochlorothienopyrimidine (AT-6-1)

Amination of bromochlorothienopyrimidine (AT-6-2)

Amination of bromochlorothienopyrimidine (AT-6-3)

Amination of bromochlorothienopyrimidine (AT-6-4)

Amination of chlorobromothienopyrimidine (AT-6-5)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (AEW 100-1) (unsuccessful)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (AEW 100-2) (unsuccessful)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (AEW 100-3)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (AEW 100-4)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (AEW 100-5)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-1)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-2)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-3)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-4)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-5)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-6)

Synthesis of 6-Bromothieno[3,2-d]pyrimidin-4-amine (CT 3-7)

Biological Evaluation

Single Shot Potencies for Compounds Submitted to GSK

Synonyms

AT 6, JRC 40, AEW 100, CT 3

 

BrC1=CC2=NC=NC(N)=C2S1

InChI=1S/C6H4BrN3S/c7-4-1-3-5(11-4)6(8)10-2-9-3/h1-2H,(H2,8,9,10)

VKZWSZNMIMJBJX-UHFFFAOYSA-N

6-bromothieno[3,2-d]pyrimidin-4-amine

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