Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-(Pyridin-3-yl)-1,3,4-thiadiazol-2-amine | HCID 199037 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86662604 | HCID 86662604 | 80% |
Reaction Steps
To a solution of aqueous hydrobromic acid (48%, 17 mL) at 5° C. in an ice bath was added 5-pyridin-3-yl-[1,3,4]thiadiazol-2-ylamine (6 g, 33 mmol) followed by bromine (12.8 mL, 0.24 mol) at a rate such that the reaction mixture was kept at a temperature below 11° C. A solution of sodium nitrite (6 g, 85 mmol) in water (8.5 mL) was added at a rate such that the reaction mixture maintained a temperature of around 5° C. The reaction mixture was kept at 2° C. for 2 hours, and then made basic to pH 8.9 using dilute NaOH at a rate needed to maintain the temperature between 5° C. and 15° C. The resulting solids were collected by filtration, washed with ice-cold water (200 mL) until filtrate was acidic (pH 4), and dried in vacuo at 35° C. to afford the title compound as an orange powder (8.68 g, 80%): mp 124-129° C.; IR (KBr thin film) 1374, 1026 cm−1; 1H NMR (300 MHz, DMSO-d6) δ 9.17 (d, J=1.8 Hz, 1H), 8.80 (dd, J=4.5, 0.9 Hz, 1H), 8.42 (dt, J=8.4, 1.8 Hz, 1H), 7.67 (ddd, J=7.2, 4.8, 0.9 Hz, 1H); ESIMS m/z 244 (M+2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912338B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-466ee06745c743ba9271f43603d7ce2a |
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| Source note | uspto-grants-2014_12 |
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