HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272246Generated: October 26, 2026
Dimethylamine → 3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester
https://huagongshe.com/reaction/1272246
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | methyl 3-formyl-1H-indole-6-carboxylate | HCID 735867 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Ammonia methanol | HCID 21705897 | 20% |
| Product | 3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester | HCID 69516454 | 99% |
Reaction Steps
A solution of methyl 3-formylindole-6-carboxylate (8.0 g, 39.3 mmol) in 270 ml methanol is treated with dimethylamine (40% aqueous; 267 ml, 2.56 mol) at ambient temperature. After 45 minutes, NaBH4 (4.45 g, 118.1 mmol) is added, and the resulting mixture is heated at 55° C. for 3 hours. The reaction mixture is allowed to cool then is diluted with CHCl3 (200 ml) and brine (150 ml). The organic layer is washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude residue is purified by flash chromatography (SiO2; 100% ethyl acetate then 20% 2M NH3/methanol in CHCl3) to give 9.07 g of 3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester (99%). Amine 61 is prepared from 3-dimethylaminomethyl-1H-indole-6-carboxylic acid methyl ester by essentially following the procedures detailed in Amine 49, 1st paragraph; and Amine 51, 3rd paragraph.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208505B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-2595965355ff47e19b1d69e5f4a9dd03 |
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| Source note | uspto-grants-2007_04 |
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