Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 22646996—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl octahydro-1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 54595540101.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273028B2
Source datasetuspto-grants-2016_03
ORD IDord-b20bc758dff6405086370c910e68e696
Source noteuspto-grants-2016_03