HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-5-nitrothiazole → HCID 2743678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-5-nitrothiazole | HCID 18211 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 22132820 | HCID 22132820 | — |
| Product | HCID 2743678 | HCID 2743678 | — |
Reaction Steps
The title compound was prepared in the manner described in Example 1. Substituting the acid chloride of thiophene-2-carboxylic acid (prepared from the acid and oxalyl chloride) for the benzoyl chloride in Example 1 gave the thiosemicarbazide of thiophene-2-carboxylic acid and then 3-(thien-2-yl)-1,2,4-triazole-5-thione. Reaction of 1.73 g of the sodium salt of the thione with 2.09 g of 2-bromo-5-nitrothiazole as in Example 1 yielded 1 g of 3-[(5-nitrothiazol-2-yl)mercapto]-5-(thien-2-yl)-1,2,4-triazole, an orange solid, MP 179°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05798374 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-795ebbb5cea6462a9fe5041f7c74bd7a |
| Source note | uspto-grants-1998_08 |