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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693392Generated: October 31, 2026

Methyl iodide → HCID 59753624, compound

https://huagongshe.com/reaction/1693392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 53255592HCID 53255592—
SolventDimethylformamideHCID 6228—
ProductHCID 59753624HCID 59753624—

Reaction Steps

To a solution of 4-(2-nitrobenzenesulfonylamino)piperidine-1-carboxylic acid tert-butyl ester (Preparation 73) (400 mg, 1.04 mmol) in DMF (10 mL) was added caesium carbonate (507 mg, 1.56 mmol) and the mixture stirred at rt for 40 min. Iodomethane (323 μL, 5.19 mmol) was added and the mixture stirred for 16 h. Solvent was removed in vacuo and the crude residue partitioned between ethyl acetate (20 mL) and water (20 mL). The organic layer was separated and washed with 1M HCl (2×20 mL), water (20 mL), then brine (2×20 mL) before being dried (MgSO4). The solvent was removed in vacuo to give the title compound as a yellow powder. δH (d6 DMSO): 8.43 (2H, m), 8.01 (2H, m), 4.00-3.89 (3H, m), 2.83-2.67 (5H, m), 1.54-1.43 (2H, m), 1.39 (9H, s), 1.34-1.24 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-989682c5b97f40fd91f29285a962bd43
Source noteuspto-grants-2012_04