Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 18975307 | HCID 18975307 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 86753096 | HCID 86753096 | 19% |
Reaction Steps
To a suspension of 3-(5-(1,2,4-triazol-4-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl)propionic acid (0.23 g) in dry DMF (3 mL) was added 1-benzylpiperazine (0.1 mL, 0.58 mmol), 1-hydroxybenzotriazole (66 mg, 0.49 mmol), 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide hydrochloride (93 mg, 0.49 mmol) and triethylamine (68 μL, 0.4 mmol) and this mixture was stirred at ambient temperature under nitrogen for 24 hours. The solvent was evaporated in vacuo and the residue partitioned between ethyl acetate (25 mL) and water (20 mL). The two phases were separated and the aqueous phase was extracted with ethyl acetate (3×25 mL). The combined organics were dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica eluting with 90:10:1, DCM:MeOH:NH3 to give the title compound (30 mg, 19%) as a colourless solid. mp 185° C. (dec.). 1H NMR (360 MHz, CDCl3 :d4 -MeOH 9:1) δ 2.29-2.34 (2H, m), 2.35-2.42 (2H, m), 2.70 (2H, t, J=7.4Hz), 3.12 (2H, t, J=7.4Hz), 3.36-3.43 (2H, m), 3.48 (2H, s), 3.58-3.64 (2H, m), 7.24-7.35 (5H, m), 7.37 (1H, s), 7.67 (1H, s), 8.60 (1H, s) and 8.93 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807857 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-091302ab33b849f1be320de000b1f96f |
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| Source note | uspto-grants-1998_09 |
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