HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014864Generated: October 26, 2026
N-Methylbutylamine → 3-(Butyl(methyl)carbamoyl)benzoic acid
https://huagongshe.com/reaction/1014864
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylbutylamine | HCID 8068 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Methoxycarbonyl)benzoic acid | HCID 601880 | — |
| Reactant | N-Boc-cis-4-hydroxy-D-proline | HCID 688616 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Methyl 3-(butyl(methyl)carbamoyl)benzoate | HCID 67316285 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Butyl(methyl)carbamoyl)benzoic acid | HCID 43452775 | — |
Reaction Steps
Step F (1): Methyl 3-(butyl(methyl)carbamoyl)benzoate. To a solution of 3-(methoxycarbonyl)benzoic acid (1.8 g, 10 mmol) in dichloromethane (40 mL) and DMF (20 mL) was added Hunig's base (2.58 g, 20 mmol) to make a clear solution and HATU (4.18 g, 11 mmol) was then added. After stirring for 10 min, the reaction mixture was added methylbutylamine (1.13 g, 13 mmol) and the reaction mixture was stirred at rt for 3 h. Dichloromethane was removed and ethyl acetate (300 mL) was added and the mixture was washed with 1N HCl, sodium carbonate solution, H2O, dried and concentrated to give the title compound ready for next step without purification: 1H NMR (CDCl3, 500 MHz) δ 0.79-0.98 (3H, m), 1.15 (1H, m), 1.41 (1H, brd s), 1.52 (1H, brd s), 1.64 (1H, m), 2.92-3.07 (2H, m), 3.21 (1H, brd s), 3.53 (1H, brd s), 3.91 (3H, s), 7.47 (1H, m), 7.58 (1H, d, J=10 Hz), 8.05-8.07 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981913B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-d740f9aef3c8455fa70e80478d056946 |
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| Source note | uspto-grants-2011_07 |
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