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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183528Generated: October 30, 2026

Thionyl Chloride → HCID 131724951, compound

https://huagongshe.com/reaction/2183528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 131724952HCID 131724952—
SolventDichloromethaneHCID 6344—
ProductHCID 131724951HCID 13172495178%

Reaction Steps

A suspension of [1-methyl-5-({[3-(5-methylisoxazol-3-yl)-[1,2,4]triazolo[3,4-α]phthalazin-6-yl]oxy}methyl]-1H-[1,2,4]triazol-3-yl}methanol (350 mg, 0.9 mmol) in dichloromethane (15 ml) was treated portionwise with thionyl chloride (5 ml) at room temperature for 1 h. The mixture was evaporated in vacuo and the residue partitioned between 5% MeOH/DCM and water. The aqueous layer was basified with saturated K2CO3 solution. The organic layer was separated, dried (MgSO4), and concentrated to give the title compound as a white solid (0.28 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900209B2
Source datasetuspto-grants-2005_05
ORD IDord-366e17feae294e3c9e6d59386f01a69a
Source noteuspto-grants-2005_05