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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859178Generated: October 30, 2026

Oxalyl chloride → HCID 15980920, compound

https://huagongshe.com/reaction/859178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Azidobenzoic acidHCID 3034184—
ReactantHCID 18619165HCID 18619165—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15980920HCID 1598092041%

Reaction Steps

To a mixture of 4-azidobenzoic acid (200 mg, 1.23 mmol) and oxalyl chloride (5 mL) was added a catalytic quantity of DMF (50 μL). The reaction mixture was stirred for 20 minutes and was concentrated in vacuo. Benzene (20 mL) was added and the mixture was again concentrated in vacuo. The resulting residue was dissolved in DCM (5 mL) and was treated with (5-amino-pyridin-2-yloxy)-acetic acid methyl ester (242 mg, 1.33 mmol) followed by DIPEA (427 μL, 2.46 mmol). The reaction mixture was stirred for 15 h at ambient temperature before being diluted with DCM, washed with water and brine and dried over magnesium sulfate. Filtration and concentration in vacuo gave a residue that was taken up in a small portion of ethyl acetate (5 mL) and was precipitated through the addition of hexanes (50 mL). The solids were collected by vacuum filtration on a fritted glass funnel to afford 164 mg (41%) of (5-(4-azido-benzoylamino)pyridin-2-yloxy)acetic acid methyl ester as a solid: 1H NMR (300 MHz, DMSO-d6) δ 10.25 (bs, 1H), 8.39 (m, 1H), 8.00 (m, 3H), 7.24 (m, 2H), 6.92 (m, 1H), 4.87 (s, 2H), 3.63 (s, 3H); MS (EI) m/z 326.12 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151112B1
Source datasetuspto-grants-2006_12
ORD IDord-b22d72c1fc584095a3204ee0bc8ad297
Source noteuspto-grants-2006_12