Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273541Generated: October 31, 2026

Pyridine → HCID 57500372, compound

https://huagongshe.com/reaction/2273541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 57500373HCID 57500373—
ReactantHCID 131733386HCID 131733386—
SolventDichloromethaneHCID 6344—
ProductHCID 57500372HCID 5750037238%

Reaction Steps

4.43 ml (43.7 mmol) of pyridine and 8.95 g (21.9 mmol) of tert-butyl[2-(3-{[(2-methylindolizin-1-yl)amino]-carbonyl}phenoxy)ethyl]carbamate are added to the suspension of 9.27 g (24.0 mmol) of benzyl 5-(chlorocarbonyl)-2-[(trifluoroacetyl)amino]benzoate in 180 ml of dichloromethane. The reaction medium that has turned greenish is stirred at ambient temperature for 16 hours. It is concentrated to dryness and the residue is taken up in diisopropyl ether and ethanol. The solid in suspension is filtered, washed with diisopropyl ether and dried. 6.29 g (38%) of a yellow powder are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120819B2
Source datasetuspto-grants-2015_09
ORD IDord-00e37e7f44c94954b5dd36ebff422c9f
Source noteuspto-grants-2015_09