HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404089Generated: October 30, 2026
Diisopropylethylamine → ethyl 2-(1-acetyl-5-bromo-7-fluoro-4-methoxy-1H-indol-3-yl)acetate
https://huagongshe.com/reaction/1404089
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (Z)-ethyl 4-(N-(2,4-dibromo-6-fluoro-3-methoxyphenyl)acetamido)but-2-enoate | HCID 86654327 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-(1-acetyl-5-bromo-7-fluoro-4-methoxy-1H-indol-3-yl)acetate | HCID 66927067 | 79.4% |
Reaction Steps
To the solution of 8-7 (20 g, 44.0 mmol) in anhydrous DMF (250 mL) was added Pd(OAc)2 (2.0 g, 8.8 mmol), Bu4NBr (14.3 g, 44.0 mmol) and DIPEA (14.2 g, 110 mmol) under N2. The mixture was stirred at 80° C. for 3 h. TLC showed that the reaction was completed. The mixture was poured into ice water and extracted with ethyl acetate (150 mL×3). The organic layers were combined and were concentrated in vacuo. The residue was purified by flash chromatography (Silica-gel, petroleum ether/ethyl acetate=10:1) to afford 8-8 (13.0 g, 79%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912220B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d372ba9c457242758dd574ed08edbc0c |
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| Source note | uspto-grants-2014_12 |
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