HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25502Generated: October 23, 2026
Acetic Acid → [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4-methoxy-benzyl)-amine
https://huagongshe.com/en/reaction/25502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamine | HCID 9943439 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(4-methoxy-benzyl)-amine | HCID 10294027 | 46.3% |
Reaction Steps
4-Methoxybenzaldehyde (0.204 g, 1.5 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.405 g, 1.48 mmol) in methylene chloride (125 mL), followed by acetic acid (0.3 g, 1.5 mmol). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.31 g, 1.46 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 3 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken, the organic layer separated and dried over Na2SO4. The solvent was evaporated to give a yellow oil. Recrystallization from methanol/water gave the product as off-white crystals (270 mg); mp 173-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858739B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-5446955f4f5346a18a8e2ea598f19e1b |
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| Source note | uspto-grants-2005_02 |
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