HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-6-cyanobenzo[d]thiazole-2-thiolate potassium salt → 4-Bromo-2-(methylthio)benzo[d]thiazole-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-6-cyanobenzo[d]thiazole-2-thiolate potassium salt | HCID 86681165 | — |
| Reactant | HCID 178469699 | HCID 178469699 | — |
| Product | 4-Bromo-2-(methylthio)benzo[d]thiazole-6-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952058B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-accddcf3b8c54430a76a17fbd324a587 |
| Source note | uspto-grants-2015_02 |