HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905709Generated: October 29, 2026
Hydrochloric Acid → 2-[2-(2-diethylaminoethylamino)ethyl]-4-methyl-1H-pyrrole-3-carboxylicacid ethyl ester
https://huagongshe.com/reaction/905709
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-[(2-diethylaminoethylcarbamoyl)methyl]-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 66607854 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(2-diethylaminoethylamino)ethyl]-4-methyl-1H-pyrrole-3-carboxylicacid ethyl ester | HCID 49840468 | 101.6% |
Reaction Steps
A stirred solution of 2-[(2-diethylamino-ethylcarbamoyl)-methyl]-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (310 mg, 1 mmol) in anhydrous tetrahydrofuran (2 ml) was added dropwise slowly with 1M borane-tetrahydrofuran complex in tetrahydrofuran (3 ml, 3 mmol) under an argon atmosphere. Upon completion of the addition, the mixture was stirred at room temperature for 1 hour and heated to reflux for another 5 hours. The reaction mixture was added with cold water (5 ml) and 1N hydrochloric acid (2 ml) dropwise, the mixture was stirred for 5 minutes, adjusted to pH 10 with 10% aqueous sodium hydroxide solution and extracted with ethyl acetate (10 ml×5). The combined organic extracts were washed with brine (15 ml), dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-[2-(2-diethylamino-ethylamino)-ethyl]-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (300 mg) as a brown oil which was used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012966B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a4135769f69442e789030f45a5647625 |
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| Source note | uspto-grants-2011_09 |
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