HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloropyridazin-3-ol → 6-Chloro-2-methyl-2,3-dihydropyridazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloropyridazin-3-ol | HCID 252828 | — |
| Reactant | 6-Chloro-2-methyl-2,3-dihydropyridazin-3-one | HCID 2783607 | — |
| Reactant | 2,2-dimethyl-3-((R)-2-oxo-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-6-yl)propanenitrile | HCID 59635685 | — |
| Product | 6-Chloro-2-methyl-2,3-dihydropyridazin-3-one | HCID 2783607 | — |
| Product | HCID 44512035 | HCID 44512035 | — |
Reaction Steps
The title compound was prepared from 2,2-dimethyl-3-((R)-2-oxo-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-6-yl)propanenitrile and 6-chloro-2-methylpyridazin-3(2H)-one following a procedure analogous to that described in Example 1 Step 3. 6-chloro-2-methylpyridazin-3(2H)-one was prepared from 6-chloropyridazin-3-(2H)-one following a procedure analogous to that described in Example 1 Step 2. LC-MS Method 2 tR=1.138 min, m/z=471.3; 1H NMR (CDCl3) 1.28 (s, 3H), 1.41 (s, 3H), 1.49 (m, 3H), 2.1 (s, 2H), 2.2 (m, 1H), 2.42 (m, 2H), 2.85 (m, 1H), 3.78 (s, 3H), 6.92 (m, 3H), 7.31 (m, 5H), 7.43 (d, 2H), 7.50 (d, 1H), 7.35 (m, 8H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592410B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-7f45304120a6473fb821bce2aee40565 |
| Source note | uspto-grants-2013_11 |