HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → 1-(Pyridazin-3-yl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | N-methoxy-N-methylpyridazine-3-carboxamide | HCID 58197546 | — |
| Product | 1-(Pyridazin-3-yl)ethan-1-ol | HCID 15197511 | 157.4% |
Reaction Steps
According to a similar synthesis of compound 4 described in Example 346, compound 1 (500 mg, 1.17 mmol) was alkylated with 1-Bromo-2-methoxy-ethane (180 mg, 1.3 mmol) to give compound 2 (360 mg, 65%) as a white solid. Compound 2 (200 mg, 0.43 mmol) was reacted with Lawesson's Reagent (190 mg, 0.47 mmol) to give compound 3 (84 mg, 50%) as a white solid. And compound 3 (80 mg, 0.17 mmol) was converted to hydantoin 4 (55 mg, 70%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212153B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-5a8201ebf0a646d68d9352fd16f5d4ec |
| Source note | uspto-grants-2015_12 |