HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919630Generated: October 31, 2026
tert-Butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylate → tert-Butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate
https://huagongshe.com/reaction/919630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylate | HCID 22646996 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate | HCID 54595540 | 101.8% |
Reaction Steps
To a solution of tert-butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylate (0.5 g, 2.3 mmol) in AcOH (15 mL) was added PtO2 (0.25 g, 1.1 mmol). The mixture was treated with an atmosphere of hydrogen atmosphere (60 psi) and stirred for 12 h at rt. The suspension was filtered through a pad celite and concentrated in vacuo to afford a residue. The crude material was diluted with ethyl acetate (50 mL) and washed with sat. NaHCO3 (100 mL), the organic phase was separated, dried (Na2SO4) filtered and concentrated in vacuo to afford the title compound (0.53 g, 99% yield). 1H NMR (400 MHz, CDCl3) δ=6.07-5.58 (m, 1H), 4.03-3.68 (m, 1H), 3.57-3.22 (m, 3H), 3.05-2.66 (m, 2H), 2.49-2.19 (m, 1H), 1.96 (s, 4H), 1.77-1.64 (m, 1H), 1.45 (s, 9H). LC/MS (m/z): calc; d. For C12H22N2O2 (M+1H) 227. found 227.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273028B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-b20bc758dff6405086370c910e68e696 |
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| Source note | uspto-grants-2016_03 |
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