HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84574Generated: October 27, 2026
Cyanogen Bromide → 5-(8-bromo-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)-4-(2-chlorophenyl)-4H-1,2,4-triazol-3-amine
https://huagongshe.com/reaction/84574
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 178514378 | HCID 178514378 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(8-bromo-4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)-4-(2-chlorophenyl)-4H-1,2,4-triazol-3-amine | HCID 57900202 | 21% |
Reaction Steps
A solution of crude 8-bromo-N-(2-chlorophenyl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carbohydrazonamide (195, 0.434) in methanol (5 mL) was treated with a solution of cyanogen bromide (115 mg, 1.1 mmol) in methanol (1 mL) at room temperature. The reaction vessel was sealed and heated at 45° C. for 2 h, cooled to room temperature, quenched upon addition of saturated sodium bicarbonate and extracted with ethylacetate. The combined organics were dried over sodium sulfate and concentrated and the residue purified by flash column chromatography (1-10% MeOH in methylene chloride to give 287 (43 mg, 21% yield). MS (ESI): 475.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846762B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-3a945639460948228bebf728b8b0da12 |
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| Source note | uspto-grants-2014_09 |
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