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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990221Generated: October 29, 2026

Pyridine → HCID 53629666, compound

https://huagongshe.com/reaction/1990221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Methylpyrazin-2-amineHCID 313215—
Reactant3-Benzyloxy-5-isopropoxybenzoic acidHCID 53401103—
SolventDichloromethaneHCID 6344—
ProductHCID 53629666HCID 5362966673.1%

Reaction Steps

Oxalyl chloride (2.1 mL, 24.0 mmol) was added to a solution of 3-[(1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid (5.72 g, 20.0 mmol) in DCM (100 mL) and the mixture stirred at ambient RT for 4 hours. The mixture was evaporated in vacuo to a residue, which was taken up in DCM (25 mL) and added to a stirred mixture of 2-amino-5-methylpyrazine (2.29 g, 21.0 mmol) and pyridine (1.94 mL, 24.0 mmol) in DCM (100 mL) at 5° C.-10° C. The mixture was stirred at RT for 18 hours, the DCM evaporated in vacuo to a residue, which was partitioned between water (50 mL) and ethyl acetate (150 mL). The organic layer was washed with brine, dried (MgSO4) and evaporated to a residue which was chromatographed on silica, eluting with 30% ethyl acetate in isohexane, and crystallised from ethyl acetate/isohexane to give the desired compound (5.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642259B2
Source datasetuspto-grants-2010_01
ORD IDord-c7b4f7e33e1b4bb9a5a2bbb09b274ab9
Source noteuspto-grants-2010_01