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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648596Generated: October 28, 2026

HCID 20144978, compound → HCID 20145027, compound

https://huagongshe.com/reaction/648596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20144978HCID 20144978—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 20145027HCID 2014502727.1%

Reaction Steps

Potassium tert-butoxide (1.46 g) was added to a solution of 2-methylamino-5-(4-pyridyl)-4-thiazolecarbaldehyde (1.9 g) and methyltriphenylphosphonium bromide (4.66 g) in dimethyl sulfoxide (87 ml) and the mixture was stirred for 5 hours at ambient temperature. The reaction mixture was poured into ice-water (300 ml) and extracted with ethyl acetate (100 ml×2). The extract was washed with a saturated aqueous solution of sodium chloride (100 ml) and dried over magnesium sulfate. Solvent was distilled off and the residue was subjected to column chromatography on silica gel (120 g) and eluted with a mixture of chloroform and methanol (40:1). The fractions containing the object compound were combined and concentrated until the volume was about 15 ml. The resultant white needles were collected by filtration and washed with cold ethyl acetate and dried under reduced pressure to give white needles of 2-methylamino-5-(4-pyridyl)-4-vinylthiazole (510 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735957
Source datasetuspto-grants-1988_04
ORD IDord-1082431640054c78b2700504828866f8
Source noteuspto-grants-1988_04