HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054679Generated: October 25, 2026
Ethyl Acetate → methyl 6-chloro-5-{4-[(2S)-pyrrolidin-2-ylmethoxy]phenyl}-1H-indole-3-carboxylate
https://huagongshe.com/reaction/1054679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2S)-2-[(4-Bromophenoxy)methyl]pyrrolidine | HCID 28750222 | — |
| Reactant | methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate | HCID 86698665 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | methyl 6-chloro-5-{4-[(2S)-pyrrolidin-2-ylmethoxy]phenyl}-1H-indole-3-carboxylate | HCID 86698682 | 71.2% |
Reaction Steps
A mixture of methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (80 mg, 0.146 mmol), (S)-2-((4-bromophenoxy)methyl)pyrrolidine (77 mg, 0.3 mmol), 2.0 M aqueous potassium carbonate (0.5 mL, 1.0 mmol), and Pd(dppf)Cl2 (10 mg, 0.01 mmol) in toluene/ethanol (1.44 mL/0.48 mL) was stirred at 110° C. for 2.5 hours. The mixture was poured into ethyl acetate and washed with water. The organic phase was dried over sodium sulfate, filtered, and concentrated to give a residue, which was purified by preparative TLC to give the title compound (40 mg, 42% yield) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.92 (s, 1 H), 7.80 (s, 1 H), 7.55 (s, 1 H), 7.45 (d, 2 H), 6.85 (d, 2 H), 4.10 (m, 1 H), 3.75 (s, 3 H), 3.65 (m, 1 H), 3.52 (m, 1 H), 3.05 (m, 2 H), 2.05 (m, 1 H), 1.90 (m, 2 H), 1.70 (m, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394285B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ff3fd52233324edb8c5769fd8d8d1a3a |
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| Source note | uspto-grants-2016_07 |
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