HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535446Generated: October 30, 2026
3-(Methoxycarbonyl)benzeneboronic acid → Methyl 2-amino-5-({1-[3-(methoxycarbonyl)phenyl]-2-methylindolizin-3-yl}carbonyl)benzoate
https://huagongshe.com/reaction/535446
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Methoxycarbonyl)benzeneboronic acid | HCID 2734714 | — |
| Reactant | Potassium phosphate dihydrate | HCID 23436936 | — |
| Reactant | Methyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoate | HCID 57500395 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water 1,2-dimethoxyethane | HCID 18180031 | — |
| Product | Methyl 2-amino-5-({1-[3-(methoxycarbonyl)phenyl]-2-methylindolizin-3-yl}carbonyl)benzoate | HCID 66653153 | 65.9% |
Reaction Steps
0.229 g (1.27 mmol) of [3-(methoxycarbonyl)phenyl]boronic acid, 0.492 g (2.12 mmol) of potassium phosphate dihydrate and 0.024 g (0.02 mmol) of tetrakis(triphenylphosphine)palladium are added, under an argon atmosphere at ambient temperature, to 0.410 g (1.06 mmol) of methyl 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoate in 8 ml of a DME/H2O (5/1) mixture. The reaction medium is heated at 90° C. for 18 hours. The reaction medium is extracted with dichloromethane, washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate, filtered, and then concentrated under reduced pressure. The solid obtained is purified by silica gel column chromatography, elution being carried out with dichloromethane. 309 mg of a yellow solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859544B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ca3aab6099ff4c8bba625c3ea634d623 |
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| Source note | uspto-grants-2014_10 |
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