HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408589Generated: October 30, 2026
Sulfuric acid magnesium salt (1:1) → 6-[(3-Ethoxycarbonyl-propylamino)-methyl]-indole-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/408589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Aminobutyrate ethyl hydrochloride | HCID 12649661 | — |
| Reactant | Tert-butyl 6-formyl-1H-indole-1-carboxylate | HCID 14616867 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-[(3-Ethoxycarbonyl-propylamino)-methyl]-indole-1-carboxylic acid tert-butyl ester | HCID 70557862 | — |
Reaction Steps
To a solution of 4-amino-butyric acid ethyl ester hydrochloride (1 eq.) in either MeOH or EtOH were added TEA (2.5 eq.), 6-formyl-indole-1-carboxylic acid tert-butyl ester (0.95 eq.) and MgSO4 (1.5 eq.). The reaction was stirred at 20° C. for 15 h, then cooled to −15° C. NaBH4 (2 to 6 eq.) was added portionwise. The reaction was stirred for 1 h at −15° C., then 1 h at 0° C. The reaction was quenched with the addition of cold water at 0° C. The crude was extracted three times with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure at 20° C. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 1/0 to 99/1) to afford 6-[(3-ethoxycarbonyl-propylamino)-methyl]-indole-1-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759334B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-8e6cc5d960eb4dc8a9f042f556ac79f3 |
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| Source note | uspto-grants-2014_06 |
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