HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 136335775, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 68920361 | HCID 68920361 | — |
| Reactant | 3H-1,2,4-Triazol-3-one, 5-(chloromethyl)-1,2-dihydro- | HCID 135546685 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136335775 | HCID 136335775 | — |
Reaction Steps
After reconversion to the base, the compound obtained in Step C of Example 1 (2.14 mmol) is dissolved in 30 ml of dimethylformamide. There are added 0.75 ml (4.28 mmol) of diisopropylethylamine and 314 mg (2.35 mmol) of 5-(chloromethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one prepared according to the method described in Tetrahedron Letters, 2000, 41, 8661. The mixture is stirred for 12 hours at ambient temperature and then evaporated to dryness. The residue obtained is taken up in dichloromethane, washed, dried, filtered and evaporated. The oil obtained is purified by flash chromatography on silica to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612061B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-2c87197585444fc8a864d8e4bfcdd314 |
| Source note | uspto-grants-2009_11 |