HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405092Generated: November 2, 2026
Methyl 4-(chlorocarbonyl)benzoate → HCID 67356193, compound
https://huagongshe.com/reaction/2405092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-(chlorocarbonyl)benzoate | HCID 81850 | — |
| Reactant | HCID 67357244 | HCID 67357244 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67356193 | HCID 67356193 | 87.9% |
Reaction Steps
A mixture of tert-butyl 3-bromo-1-ethyl-1H-pyrrolo[3,2-c]pyridin-6-ylcarbamate (3C, 340 mg, 0.99 mmol) in 4M HCl in dioxane (3 ml) was stirred at room temperature for 1 h and 70° C. for 2 h. The mixture was concentrated in vacuo and dissolved in pyridine (3 ml). To the mixture, methyl 4-(chlorocarbonyl)benzoate (220 mg, 1.1 mmol) was added and stirred at room temperature for 3 h. The mixture was extracted with EtOAc/H2O. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude mixture was purified by chromatography (basic-SiO2, hexanes:EtOAc=3:1) to give methyl 4-(3-bromo-1-ethyl-1H-pyrrolo[3,2-c]pyridin-6-ylcarbamoyl)benzoate (3D, 350 mg, 0.87 mmol, 87% yield) as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.40 (t, J=1.00 Hz, 3H) 3.90 (s, 3H) 4.21 (q, J=7.16 Hz, 2H) 7.72 (s, 1H) 7.99-8.11 (m, 2H) 8.11-8.20 (m, 2H) 8.35 (d, J=0.76 Hz, 1H) 8.52 (d, J=1.01 Hz, 1H) 10.96 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802695B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-935809593eee49e79f20b6b1bee7467b |
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| Source note | uspto-grants-2014_08 |
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