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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531957Generated: October 26, 2026

Sodium Cyanide → N-(1-acetyl-5-cyanomethyl-4,6-dimethylindolin-7-yl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/1531957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantIndolineHCID 10328—
ReactantCyanic acid, methyl esterHCID 137201—
ReactantN-(1-Acetyl-5-chloromethyl-4,6-dimethylindolin-7-yl)-2,2-dimethylpropanamideHCID 15895572—
Catalyst18-Crown-6HCID 28557—
SolventAcetonitrileHCID 6342—
ProductN-(1-acetyl-5-cyanomethyl-4,6-dimethylindolin-7-yl)-2,2-dimethylpropanamideHCID 15524343—

Reaction Steps

1.27 (9H, S, C(CH3)3), 2.25 (3H, s, -CH3), 2.30 (6H, s, -CH3, >NCOCH3), 3.00 (2H, br, Indoline C3—H), 4.05 (2H, br, Indoline C2—H), 4.68 (2H, s, -CH2c l), 9.16 (1H, br, >NH). (3) N-(1-Acetyl-5-chloromethyl-4,6-dimethylindolin-7-yl)-2,2-dimethyl-propanamide (21 g) was suspended in CH3CN (150 ml), and NaCN (8.1 g) and 18-crown-6 (870 mg) were added, which was followed by refluxing for 15 hr. CH3CN was evaporated under reduced pressure and CHCl3 (300 ml) was added. The mixture was washed with water and dried over anhydrous sodium sulfate. CHCl3 was evaporated under reduced pressure. The obtained residue was washed with boiling MeOH to give 15.5 g of N-(1-acetyl-5-cyanomethyl-4,6-dimethylindolin-7-yl)-2,2-dimethylpropanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200988B1
Source datasetuspto-grants-2001_03
ORD IDord-56054b5cf45e428ca0a22880c95415e0
Source noteuspto-grants-2001_03