Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 5-Chloro-1H-indole-2-carboxylic acid | HCID 82693 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58775951 | HCID 58775951 | — |
Reaction Steps
EDCI (0.33 mmol, 0.07 g) was added in one portion to a suspension of Compound 14c (0.25 mmol, 0.05 g), 5-chloro-1H-indole-2-carboxylic acid Compound 14d (0.22 mmol, 0.04 g) and HOBt (0.22 mmol, 0.03 g) in DMF (5.0 mL) at 0° C. The resulting suspension was warmed to r.t. and then a crystal of DMAP and Et3N (0.65 mmol, 0.1 mL) was added and the reaction mixture was stirred overnight. The resulting orange-yellow suspension was poured in water and was extracted with EtOAc (25 mL). The organic layer was washed with water (2×20 mL) followed by 5% NaOH solution (10 mL) and brine. The organic layer was separated, dried over Na2SO4 and filtered. The solvent was removed in vacuo and the resulting residue was purified by preparative TLC (15:1 CH2Cl2/MeOH) to yield 5-chloro-1H-indole-2-carboxylic acid {4-[(cyclohexyl-methyl-amino)-methyl]-phenyl}-amide Compound 14e (0.06 g, 68%) as a pale yellow solid. MS m/e 396 (M+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799824B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-2d6166435ef041eb8d9187f80b6e9819 |
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| Source note | uspto-grants-2010_09 |
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