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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242664Generated: October 30, 2026

Dicyclohexylcarbodiimide → Methyl 6-chloropyridine-3-carboxylate

https://huagongshe.com/reaction/1242664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPhenyl chloroformateHCID 15891—
ReactantThionyl ChlorideHCID 24386—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-Chloronicotinic acidHCID 79222—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantCarbodiimideHCID 160435—
ReactantCarbonochloridateHCID 21226386—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl 6-chloropyridine-3-carboxylateHCID 254249—

Reaction Steps

6-Chloronicotinic acid 51 is activated by reacting with a chloroformate activating agent such as SOCl2, phenylchloroformate, or p-nitrophenyl chloroformate, or a carbodiimide activating agent such as CDI, DCC, or EDC in the presence of HOBt and N-hydroxysuccinimide in a polar aprotic solvent such as CH2Cl2, 1,2-dichloroethane, DMF, or NMP, and heating. An alcohol such as methanol is then added to form 6-chloronicotinic acid methyl ester 52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115746B2
Source datasetuspto-grants-2006_10
ORD IDord-bd06e1bc1327464fbf511b9232fe089c
Source noteuspto-grants-2006_10