HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191330Generated: November 1, 2026
Triethylamine → N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide
https://huagongshe.com/reaction/1191330
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | (2-Amino-4,5-dimethoxy-phenyl)-(3-bromo-phenyl)-methanone | HCID 7148514 | — |
| Solvent | Nitrogen | HCID 947 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide | HCID 66849274 | — |
Reaction Steps
To a solution of (2-amino-4,5-dimethoxyphenyl)(3-bromophenyl)methanone (5 g, 14.9 mmol) in dry DCM (125 mL) was added thiophen-2-ylacetic acid (2.54 g, 17.9 mmol) and Et3N (6.77, 66.9 mmol) at 0° C. in N2. 10 minutes later, POCK (3.4 g, 22.31 mmol) was added dropwise at 0° C. in N2. The reaction mixture was stirred for 1 hour at 0° C. and then quenched with saturated NaHCO3, and neutralized to pH=8. The mixture was exacted with ACM (30 mL×3). The combined organic layer was dried over anhydrous MgSO4, filtered and concentrated under vacuum to afford N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide. MS (M+H)=460 and 462.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680116B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-f6e5b460fdec4f8bb7b766f39a88414e |
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| Source note | uspto-grants-2014_03 |
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