HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579360Generated: October 25, 2026
Phosphorus oxychloride → 5-(4-Bromo-2,6-difluorophenyl)-1,3,4-thiadiazol-2-amine
https://huagongshe.com/reaction/579360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | 4-Bromo-2,6-difluorobenzoic acid | HCID 2773298 | — |
| Product | 5-(4-Bromo-2,6-difluorophenyl)-1,3,4-thiadiazol-2-amine | HCID 80132630 | 84% |
Reaction Steps
A stirred mixture of 4-bromo-2,6-difluorobenzoic acid (5 g, 21.1 mmol) and hydrazinecarbothioamide (2.88 g, 31.6 mmol) was cooled under nitrogen in an ice bath. POCl3 (5.9 mL, 63.3 mmol) was added drop-wise and the reaction was stirred at ice bath temperature for 15 minutes then heated at 78° C. for 3 hours. The reaction mixture was cooled in an ice bath then quenched by addition of ice water (150 mL). The resulting solid was sonicated for 30 minutes to give a free stirring suspension which was left to slurry at room temperature for 72 hours. The solid was collected by vacuum filtration, rinsed with water, and re-suspended in saturated NaHCO3(aq) (150 mL). This suspension was stirred at room temperature for 18 hours then the solid was collected by vacuum filtration, rinsed with water, and dried in a vacuum oven for 24 hours to give the title compound (5.174 g, 84% yield) which was used in the next step without further purification. LC-MS: Rt 0.99 min; MS m/z 294.2 [M+2]+ [Method A]. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.68 (d, J=8.08 Hz, 2H), 7.57 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040712B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-1e5f9a2e2f1148888669b25ea74fa741 |
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| Source note | uspto-grants-2015_05 |
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