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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848196Generated: October 31, 2026

4-Bromo-6-cyanobenzo[d]thiazole-2-thiolate potassium salt → 4-Bromo-2-(methylthio)benzo[d]thiazole-6-carbonitrile

https://huagongshe.com/reaction/1848196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-6-cyanobenzo[d]thiazole-2-thiolate potassium saltHCID 86681165—
ReactantHCID 178469699HCID 178469699—
Product4-Bromo-2-(methylthio)benzo[d]thiazole-6-carbonitrileHCID 86681164—

Reaction Steps

4-Bromo-2-(methylthio)benzo[d]thiazole-6-carbonitrile was synthesized as a yellow solid (1.0 g, 12%) using a procedure analogous to that described in Step 2 of Example 114, substituting 4-bromo-6-cyanobenzo[d]thiazole-2-thiolate potassium salt from the previous step for ethyl 2-mercaptothiazolo[4,5-b]pyridine-6-carboxylate potassium salt used in Example 114. LCMS (ESI) m/z 284, 286 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-accddcf3b8c54430a76a17fbd324a587
Source noteuspto-grants-2015_02