Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl nipecotate | HCID 98969 | — |
| Reactant | 2-tert-Butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazole-5-sulfonyl chloride | HCID 57937298 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57937350 | HCID 57937350 | — |
Reaction Steps
2-tert-Butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazole-5-sulfonyl chloride (400 mg, 0.98 mmol) was added to a solution of ethyl piperidine-3-carboxylate (771 mg, 4.90 mmol) and DMAP (600 mg, 4.90 mmol) in MeCN (50 mL). The reaction mixture was stirred overnight at ambient temperature and the solvent was concentrated. The product was purified by MPLC using 50-90% EtOAc/Heptane on silica gel to provide the title compound as colorless oil. Yield: 182 mg (38%); 1H NMR (400 MHz, CDCl3) δ 1.26 (t, J=7.13 Hz, 3 H), 1.29-1.38 (m, 1 H), 1.49-1.57 (m, 4 H), 1.59 (s, 9 H), 1.63-1.83 (m, 2 H), 1.91-2.02 (m, 1 H), 2.30 (td, J=11.43, 2.93 Hz, 2 H), 2.44 (t, J=11.13 Hz, 1 H), 2.57-2.69 (m, 1 H), 3.28-3.40 (m, 2 H), 3.65-3.75 (m, 1 H), 3.91 (dd, J=11.82, 3.81 Hz, 1 H), 3.96-4.05 (m, 2 H), 4.13 (q, J=7.03 Hz, 2 H), 4.25 (d, J=7.23 Hz, 2 H), 7.43 (d, J=8.20 Hz, 1 H), 7.64 (dd, J=8.59, 1.76 Hz, 1 H), 8.19 (d, J=1.56 Hz, 1 H); MS (ESI) (M+H)+ 491.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615642B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-42fc159f79dc448b973940b7be812af8 |
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| Source note | uspto-grants-2009_11 |
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