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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416253Generated: October 31, 2026

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

https://huagongshe.com/reaction/2416253

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): δ 9.84 (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 numberUS06822100B2
Source datasetuspto-grants-2004_11
ORD IDord-dd884391c511400c89438750fc9e9439
Source noteuspto-grants-2004_11