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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368051Generated: November 1, 2026

3-Chloro-6-methylpyridazine → HCID 49793199, compound

https://huagongshe.com/reaction/2368051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-6-methylpyridazineHCID 227254—
ReactantHCID 49838825HCID 49838825—
ReactantHCID 68759713HCID 68759713—
ProductHCID 49793199HCID 49793199—

Reaction Steps

The title compound was prepared from 3-{(S)-cyclopropyl-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]methyl}-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-one {prepared in analogy to the intermediate in Example 3 from 3-[(S)-(4-bromo-phenyl)-cyclopropyl-methyl]-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-one} and 3-chloro-6-methyl-pyridazine following a procedure analogous to that described in Example 3. LC-MS (Method 1): tR=3.39 min; Mass spectrum (ESI+): m/z=472 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703765B2
Source datasetuspto-grants-2014_04
ORD IDord-04ff98ed88f849f4a9a6fbd89fe1b1e5
Source noteuspto-grants-2014_04