HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624199Generated: October 31, 2026
(1,1'-Biphenyl)-3-carboxylic acid, 3'-amino-, methyl ester → Methyl 3'-(2-(tert-butoxycarbonylamino)ethylamino)biphenyl-3-carboxylate
https://huagongshe.com/reaction/1624199
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1,1'-Biphenyl)-3-carboxylic acid, 3'-amino-, methyl ester | HCID 1394215 | — |
| Reactant | tert-Butyl N-(2-bromoethyl)carbamate | HCID 4103526 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3'-(2-(tert-butoxycarbonylamino)ethylamino)biphenyl-3-carboxylate | HCID 21191174 | 16.3% |
Reaction Steps
A mixture of methyl 3′-aminobiphenyl-3-carboxylate (3.0 g, 13.22 mmol, 1.00 equiv.), tert-butyl 2-bromoethylcarbamate (3.0 g, 13.22 mmol, 1.00 equiv.) potassium carbonate (3.6 g, 26.09 mmol, 2.00 equiv.), and N,N′-dimethylformamide (20 mL) was heated at 50-60° C. for about 16 hours. Additional tert-butyl 2-bromoethylcarbamate (3.0 g, 13.22 mmol, 1.00 equiv) was added and the mixture was heated an additional 14 hours. The mixture was cooled to ambient temperature and partitioned between ethyl acetate and water. The organic layer was separated, washed with water, dried over sodium sulfate, filtered, and concentrated to afford a crude product that was purified by silica gel chromatography (petroleum ether/ethyl acetate (8:1) to give the title product as light-yellow oil (800 mg; yield=16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778998B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-5711b9d4df104e9090beb83c39affc95 |
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| Source note | uspto-grants-2014_07 |
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