Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411249Generated: October 27, 2026

Cyanoacetic acid → 5-chloro-N-(5-chlorothiazol-2-yl)-1'-(2-cyanoacetyl)spiro[indoline-3,3'-pyrrolidine]-1-carboxamide

https://huagongshe.com/reaction/1411249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantHCID 71522964HCID 71522964—
Reactant5-chloro-N-(5-chlorothiazol-2-yl)spiro[indoline-3,3'-pyrrolidine]-1-carboxamideHCID 90449271—
Product5-chloro-N-(5-chlorothiazol-2-yl)-1'-(2-cyanoacetyl)spiro[indoline-3,3'-pyrrolidine]-1-carboxamideHCID 89520792—

Reaction Steps

The captioned compound was obtained in the form of a white solid by performing the same reactions and/or treatments as those in Example 23, with the exceptions that the 5-chloro-N-(5-chlorothiazol-2-yl)spiro[indoline-3,3′-pyrrolidine]-1-carboxamide obtained as an intermediate of Example 39 was used instead of 5-bromo-N-(5-chlorothiazol-2-yl)spiro[indoline-3,3′-pyrrolidine]-1-carboxamide, and that cyanoacetic acid was used instead of formic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-1a30dbd181cd4e47ac6d32878d258187
Source noteuspto-grants-2014_12