HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922145Generated: October 26, 2026
Triethylamine → 3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxy-N-(3-methoxyphenyl)-propanamide
https://huagongshe.com/reaction/922145
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxypropanoic acid | HCID 58097206 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxy-N-(3-methoxyphenyl)-propanamide | HCID 46851209 | 48% |
Reaction Steps
3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxypropanoic acid (0.025 g, 0.061 mmol) was suspended in anhydrous CH2Cl2 and cooled to 0° C. Thionyl chloride (0.005 mL, 0.073 mmol) was added dropwise and the reaction was stirred at 0° C. for 1 h. m-Anisidine (0.008 mL, 0.073 mmol) and Et3N (0.010 mL, 0.073 mmol) were added and the reaction was allowed to warm to ambient temperature over 2.5 h. Upon completion, the solution was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by chromatography (SiO2, 0-30% EtOAc/Hexane) to afford the desired product (15 mg, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278923B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-452fb9c575864e1786912c236d432602 |
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| Source note | uspto-grants-2016_03 |
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