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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009760Generated: October 30, 2026

Diethyl Ether → HCID 67305487, compound

https://huagongshe.com/reaction/1009760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantMethylamineHCID 6329—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67304717HCID 67304717—
SolventDichloromethaneHCID 6344—
ProductHCID 67305487HCID 67305487—

Reaction Steps

Oxalyl chloride (0.142 ml) was added to a mixture of N-(1-ethylpyrazol-4-yl)-2-[4-(6-carboxyquinolin-4-yloxy)-2-methoxyphenyl]acetamide (0.15 g) and methylene chloride (6 ml) and the resultant mixture was stirred at ambient temperature for 10 minutes. Diethyl ether (10 ml) was added and the resultant precipitate was recovered and dried under vacuum. The material so obtained was suspended in methylene chloride and methylamine gas was passed into the suspension until a clear solution was obtained. The solvent was evaporated and the residue was purified by column chromatography on silica using a gradient of 100:0 to 19:1 of methylene chloride and methanol as eluent. There was thus obtained the title compound (0.102 g); 1H NMR: (DMSOd6) 1.33 (t, 3H), 2.85 (d, 3H), 3.61 (s, 2H), 3.78 (s, 3H), 4.07 (q, 2H), 6.7 (d, 1H), 6.87 (m, 1H), 7.01 (d, 1H), 7.37 (d, 1H), 7.42 (s, 1H), 7.88 (s, 1H), 8.08 (d, 1H), 8.24 (m, 1H), 8.77 (d, 1H), 8.82 (q, 1H), 8.87 (d, 1H), 10.06 (s, 1H); Mass Spectrum: M+H+ 460.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973164B2
Source datasetuspto-grants-2011_07
ORD IDord-e654c6da49284ce0add0067fb61ef841
Source noteuspto-grants-2011_07