Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 22042619 | HCID 22042619 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21037779 | HCID 21037779 | — |
Reaction Steps
0.2 g of 4-[4-(benzenesulfonyl-isobutyl-amino)-phenyl]-5,5,5-trifluoro-4-hydroxy-pent-2-ynoic acid (see Example 69; 0.439 mmol) and 0.26 mL of methylamine (2M in THF) were combined in 3 mL of CH2Cl2 at rt. 0.1 g of 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.527 mmol) was added. The resulting mixture was stirred at rt for 16 h. After addition of 80 mL of CH2Cl2 the resulting solution was washed with an aqueous solution of citric acid, a saturated aqueous solution of sodium bicarbonate and brine. The organic layers were dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica(EtOAc:hexanes, 1:1) to give the title compound. 1H NMR (400 MHz, CDCl3) δ 0.90 (m, 6H), 1.56 (m, 1H), 2.91 (d, J=5.0 Hz, 3H), 3.31 (m, 2H), 3.72 (br s, 1H), 6.26 (d, 5.0 Hz, 1H), 7.11 (d, J=8.7 Hz, 2H), 7.44–7.60 (m, 5H), 7.64 (d, J=8.7 Hz, 2H). Mass Spectrum (CI+) m/e=486 (M+18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071358B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-c3bc4ba7f6bb4a54a7d11f396736f8e8 |
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| Source note | uspto-grants-2006_07 |
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