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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045997Generated: October 30, 2026

6-Chloropyridazin-3-ol → 6-Chloro-2-methyl-2,3-dihydropyridazin-3-one

https://huagongshe.com/reaction/2045997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloropyridazin-3-olHCID 252828—
Reactant6-Chloro-2-methyl-2,3-dihydropyridazin-3-oneHCID 2783607—
Reactant2,2-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)propanenitrileHCID 59635685—
Product6-Chloro-2-methyl-2,3-dihydropyridazin-3-oneHCID 2783607—
ProductHCID 44512035HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592410B2
Source datasetuspto-grants-2013_11
ORD IDord-7f45304120a6473fb821bce2aee40565
Source noteuspto-grants-2013_11