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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N,N-dimethyl-2-(indol-5-yl)cycloprop-1-yl-methylamine | HCID 67550440 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-dimethyl-2-(3-formyl-indol-5-yl)cycloprop-1-yl-methylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06822100B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-dd884391c511400c89438750fc9e9439 |
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| Source note | uspto-grants-2004_11 |
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