HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49424Generated: October 29, 2026
Water → 7,8-Difluoro-1,2,3,4-tetrahydrocyclopent[b]indol-4-yl2-propylamine fumarate
https://huagongshe.com/reaction/49424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromo-4,5-difluoroaniline | HCID 11206558 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 7,8-Difluoro-1,2,3,4-tetrahydrocyclopent[b]indol-4-yl2-propylamine fumarate | HCID 86759384 | 238.4% |
Reaction Steps
To a stirred solution of 2-bromo-4,5-difluoroaniline [H. Ishikawa, T. Uno, H, Miyamoto, H. Hiraki, H. Tamaoka, M. Tominaga and K. Nakagawa, Chem. Pharm. Bull., 1990, 38(9), 2459-2462] (72 g, 34 mmol) in ether (50 mL) at 0° C. was added sodium carbonate (5.4 g, 44 mmol) and trifluoroacetic anhydride (6.2 mL, 44 mmol). The reaction mixture was stirred at room temperature for 1 h. Water (100 mL) was added and the mixture was extracted with dichloromethane (3×100 mL). The organic extracts were combined, dried (magnesium sulfate), filtered and concentrated in vacuo to give the product (9.9 g, 94%) as a white solid. IR νmax (Nujol)/cm−1 3270, 1716, 1550, 1489, 1465, 1226, 1181, 919, 876 and 821; NMR δH (400 MHz, CDCl3) 7.45-7.5 (1H, dd, J 7.5 Hz), 8.28-8.34 (1H, dd, J 8 Hz) and 8.36 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706750B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-1a8bbcaf68f44b819ee9104b64462c13 |
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| Source note | uspto-grants-2004_03 |
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