HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235159Generated: October 30, 2026
HCID 68697948, compound → HCID 68694214, compound
https://huagongshe.com/reaction/2235159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68697948 | HCID 68697948 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 68694214 | HCID 68694214 | — |
Reaction Steps
A solution of 7-(4-ethoxycarbonyl-phenylcarbamoyl)-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester (1.1 g, 2.5 mmol) in trifluoroacetic acid (5 ml) was stirred at room temperature for 2 hours. The solvent was then removed and the residue redissolved in dichloromethane and washed with saturated sodium hydrogencarbonate. The organic layer was dried with Na2SO4 and evaporated. The residue was purified by flash chromatography (heptane/ethyl acetate gradient) to yield 4-[(1,2,3,4-tetrahydro-quinoline-7-carbonyl)-amino]-benzoic acid ethyl ester as a white solid, 790 mg (97%). MS (ISP): m/e=325.4 (M+H+.); δH (300 MHz; CDCl3) 8.59 (1H, s), 7.98 (2H, d), 7.77 (1H, s), 7.69 (2H, d), 7.48 (1H, d), 7.09 (1H, d), 4.37 (2H, q), 3.44 (2H, m), 2.79 (2H, t), 2.08 (2H, m), 1.40 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713996B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-7fd9fb8fa35a4070976e6993ff1706b7 |
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| Source note | uspto-grants-2010_05 |
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