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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893024Generated: October 30, 2026

Dimethylformamide → HCID 86745912, compound

https://huagongshe.com/reaction/893024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 10334479HCID 10334479—
ReactantHCID 10469565HCID 10469565—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 86745912HCID 86745912—

Reaction Steps

A solution of oxalyl chloride (0.4 ml) in acetonitrile (0.4 ml) is added dropwise to a solution of 1 ml of DMF and 2.4 ml of acetonitrile. The mixture is stirred (mechanically) for 15 minutes at -20° and a precipitate separates. Powdered 6-acetoxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (1.169 g, 4 mmol) is added, the mixture is stirred 20 minutes at -20°, 20 minutes at 0° and then is recooled to -20°. A solution of 1.165 g (4 mmol) of N-(2-hydroxyethyl)-N-methyl-[2,6-bis(1-pyrrolidinyl)]-4-pyrimidinamine in 1 ml of pyridine and a total of 4 ml of acetonitrile is added. The mixture is allowed to warm and stand overnight at 20°-25° and then is diluted with methylene chloride. The solution is washed with water, aqueous potassium bicarbonate and water, then dried and concentrated to give a foam. Chromatography on silica gel and elution with acetone/methylene chloride (10/90) gives the title compound. NMR 4.70, 4.27, 3.9-3.2, 2.85, 2.58, 2.32, 2.17, 2.16, 2.02, 1.9 and 1.58 δ; m.p. 69.5°-76°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120843
Source datasetuspto-grants-1992_06
ORD IDord-0218f38a32004a33add56953442ce5d2
Source noteuspto-grants-1992_06