HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890809Generated: October 27, 2026
Diisopropylethylamine → 5-(3-(3-(3-Chloro-phenyl)-propylamino)-propyl)-thiophene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/890809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3-Chlorophenyl)propionaldehyde | HCID 10419579 | — |
| Reactant | Methyl 5-(3-aminopropyl)thiophene-2-carboxylate | HCID 19989043 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(3-(3-(3-Chloro-phenyl)-propylamino)-propyl)-thiophene-2-carboxylic acid methyl ester | HCID 53900120 | 97.2% |
Reaction Steps
A solution of 5-(3-amino-propyl)-thiophene-2-carboxylic acid methyl ester (0.118 g, 0.5 mmol) and diisopropylethylamine (0.071 g, 0.55 mmol) in 10 mL MeOH was stirred at room temperature for 30 minutes and 3-(3-chloro-phenyl)-propionaldehyde (0.093 g, 0.55 mmol) was added. The mixture was stirred for 90 minutes. The reaction was cooled to 0° C., NaBH4 (0.83 mL, 5.98 mmol) was added and the mixture was stirred for 30 minutes. The reaction was quenched with 1:1 NaHCO3:H2O and was washed with CH2Cl2. The CH2Cl2 extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to afford the title compound as an oil (171 mg). MS 352 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998423B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-779d6fa0420d4b06b592db80fcdb2fea |
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| Source note | uspto-grants-2006_02 |
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