HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865501Generated: October 30, 2026
Formic Acid → 2-amino-3-(1H-indol-3-yl)-N-(2-methoxybenzyl)propanamide
https://huagongshe.com/reaction/865501
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | 3-(1H-indol-3-yl)-N-(2-methoxybenzyl)-2-(N-triphenylmethylamino)propanamide | HCID 18709616 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-amino-3-(1H-indol-3-yl)-N-(2-methoxybenzyl)propanamide | HCID 10805858 | 90% |
Reaction Steps
Formic acid (9.0 ml, 238.540 mmol) was added to a stirring solution of 3-(1H-indol-3-yl)-N-(2-methoxybenzyl)-2-(N-triphenylmethylamino)propanamide (14.11 g, 23.763 mmol) in anhydrous methylene chloride under a nitrogen atmosphere at 0° C. After 4 hours, the reaction mixture was concentrated to an oil on a rotary evaporator and redissolved in diethyl ether and 1.0N hydrochloric acid. The aqueous layer was washed twice with diethyl ether and basified with sodium hydroxide to a pH greater than 12. The product was extracted out with methylene chloride (4×). The organic extracts were combined, dried over anhydrous sodium sulfate, filtered, and concentrated on a rotary evaporator to a white foam. The compound 3-(1H-indol-3-yl)-2-amino-N-(2-methoxybenzyl)propanamide (7.52 g, 21.397 mmols) was isolated giving a 90% yield. No further purification was necessary.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565568 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-d741bb2b892e4101812447b07b0bed25 |
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| Source note | uspto-grants-1996_10 |
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