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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405220Generated: November 2, 2026

Methyl isocyanoacetate → 6-isocyano-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/2405220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl isocyanoacetateHCID 547815—
Reactant2,3-Bis(chloromethyl)pyridineHCID 14518750—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product6-isocyano-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid methyl esterHCID 87320580—

Reaction Steps

Isocyano-acetic acid methyl ester (112 mg, 1.13 mmol) and 2,3-bis-chloromethyl-pyridine (200 mg, 1.14 mmol) were dissolved in DMF. Potassium tert-butoxide (0.255 g, 2.27 mmol) was added and the reaction mixture was stirred for 1 h at room temperature. The mixture was partitioned between EA and a saturated aqueous sodium hydrogencarbonate solution, the aqueous phase extracted with EA, and the organic extracts were dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica gel chromatography (HEP/EA gradient) to give 6-isocyano-6,7-dihydro-5H-[1]pyrindine-6-carboxylic acid methyl ester. This compound was added to a solution of thionyl chloride (147 mg, 1.23 mmol) in ethanol (1 ml) and refluxed overnight. The mixture was evaporated to dryness, and the residue was stirred with HEP, filtered and dried in vacuo. The obtained product was reacted with 4-methoxy-3-(2-m-tolyl-ethoxy)-benzoic acid in analogy to step 1 of example 15 and the title compound purified by preparative RP HPLC (water/ACN gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802720B2
Source datasetuspto-grants-2014_08
ORD IDord-16c7e03f137f49f8988fec688edd3983
Source noteuspto-grants-2014_08