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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836630Generated: November 2, 2026

Dimethylformamide → N,N-dimethyl-2-(3-formyl-indol-5-yl)cycloprop-1-yl-methylamine

https://huagongshe.com/reaction/1836630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN,N-dimethyl-2-(indol-5-yl)cycloprop-1-yl-methylamineHCID 67550440—
SolventWaterHCID 962—
ProductN,N-dimethyl-2-(3-formyl-indol-5-yl)cycloprop-1-yl-methylamineHCID 22638743—

Reaction Steps

Phosphorous oxychloride (0.08 mL, 0.85 mmol, 0.91 equiv.) and dimethyl formamide (0.32 mL, 4.09 mmol, 4.4 equiv.) were combined at room temperature with stirring. After 15 min, N,N-dimethyl-2-(indol-5-yl)cycloprop-1-yl-methylamine was added dropwise in DMF (5 mL). After 2 hs of stirring at room temperature, ice and 1 N NaOH were added, then the mixture was diluted further with water and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give N,N-dimethyl-2-(3-formyl-indol-5-yl)cycloprop-1-yl-methylamine (120 mg) as an oil. 1H NMR (MeOH-d4): δ9.84 (s, 1H), 8.04 (s, 1H), 7.97 (s, 1H), 7.36 (d, J=8.4 Hz, 1H), 7.05 (dd, J=15.5, 1.7 Hz, 1H), 2.59 (dd, J=12.7, 6.7, 1H), 2.35 (s, 6H), 2.30 (m, 1H), 1.80 (m, 1H), 1.20 (m, 1H), 1.05 (m, 1H), and 0.88 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777437B2
Source datasetuspto-grants-2004_08
ORD IDord-d1ceae8de2724fa3833132048698e63e
Source noteuspto-grants-2004_08