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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527906Generated: October 31, 2026

Acetic Acid → Tert-butyl 3-(5-cyanoindolin-1-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/527906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2,3-Dihydro-1H-indole-5-carbonitrileHCID 21907639—
SolventMethanolHCID 887—
ProductTert-butyl 3-(5-cyanoindolin-1-yl)pyrrolidine-1-carboxylateHCID 66765193—

Reaction Steps

To a solution of indoline-5-carbonitrile (110 mg, 0.75 mmol) in 2.5 mL of MeOH was added tert-butyl 3-oxopyrrolidine-1-carboxylate (166 mg, 0.90 mmol) and HOAc (0.11 mL, 1.88 mmol) subsequently. After stirring at room temperature for 10 minutes, NaCNBH3 (57 mg, 0.90 mmol) was added and the mixture was then stirred at ambient temperature for 2 days. The volatiles were removed under vacuum. The residue was diluted with EtOAc, then washed with 1 N NaOH solution and brine, dried over Na2SO4, and evaporated in vacuo to afford the crude title compound for the next step use without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346810B2
Source datasetuspto-grants-2016_05
ORD IDord-937b76c122d547d294cb695a9b04a76a
Source noteuspto-grants-2016_05