HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 5,7-Dichloro-[1,2,4]triazolo[1,5-A]pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ethyl [(4,6-dichloropyridin-2-yl)carbamothioyl]carbamate | HCID 59437527 | — |
| Solvent | Ethanol, mixt. with methanol | HCID 18681192 | — |
| Product | 5,7-Dichloro-[1,2,4]triazolo[1,5-A]pyridin-2-amine | HCID 59437562 | 60% |
Reaction Steps
Ethyl [(4,6-dichloropyridin-2-yl)carbamothioyl]carbamate (2.9 g, 9.9 mmol) was added to a stirred suspension of hydroxylamine hydrochloride (1.1 g, 16 mmol) and DIEA (1.9 g, 15 mmol) in MeOH/EtOH (1:1, 40 mL) portion-wise as a solid. This mixture was stirred at rt for 2 h and then heated at 80° C. for 18 h. The reaction mixture was concentrated in vacuo and the resultant reside treated with water yielding a cream solid, which was filtered and dried in a vacuum oven at 40° C. for 18 h to give the desired product (1.2 g, 60%). 1H NMR (DMSO) δ 7.58 (d, J=2.0 Hz, 1H), 7.35 (d, J=2.0 Hz, 1H), 6.44 (s, 2H). m/z [M+H]+=203.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181234B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-143d166e301e4195b9249b690e8e7f2f |
| Source note | uspto-grants-2015_11 |