Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Ethyl 3-amino-4-[isobutyl(propyl)amino]benzoate | HCID 67528421 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67542103 | HCID 67542103 | 94% |
Reaction Steps
To a solution of ethyl 3-amino-4-[isobutyl(propyl)amino]benzoate (5 g, 0.0179 mol) in dry DCM (50 mL) was added triethyl amine (7.24 g, 0.0716 mol) at RT. Methane sulphonyl chloride (2.67 g, 0.0233 mol) was added in drops at 0° C. The reaction mixture was stirred at RT for 4 h. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in water, extracted with ethylacetate (2×75 mL), washed with 0.5M HCl, brine, dried over sodium sulphate and evaporated to afford the title compound as a yellow oil (6 g, 93%). 1H NMR (DMSO-d6, 400 MHz) δ 8.45 (s, 1H), 7.86 (s, 1H), 7.65 (m, 1H), 7.28 (m, 1H), 4.28 (m, 2H), 3.09 (s, 3H) 3.01 (m, 2H), 2.86 (m, 2H), 1.68 (m, 1H), 1.42 (m, 2H), 1.28 (m, 3H), 0.80 (m, 9H). LC/MS (Method A): 357.0 (M+H)+. HPLC (Method B) Rt 5.09 min (purity: 94.40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202865B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-969f0eab5e264e2d87ee176d7aa7ed98 |
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| Source note | uspto-grants-2012_06 |
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