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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908072Generated: November 3, 2026

N-bromobutanimide → HCID 58551010, compound

https://huagongshe.com/reaction/1908072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 58550745HCID 58550745—
SolventDichloromethaneHCID 6344—
SolventSodium ThiosulfateHCID 24477—
ProductHCID 58551010HCID 58551010—

Reaction Conditions

Temperature0 °C

Reaction Steps

To tert-butyl spiro[piperidine-4,4′-pyrrolo[2,1-c][1,4]benzoxazine]-1-carboxylate (13.2 g, 38.8 mmol) in CH2Cl2 (125 mL) at 0° C. was added NBS (7.25 g, 40.7 mmol) in CH2Cl2 (25 mL) dropwise over 10 min. The mixture was stirred at 0° C. for 5 min before it was diluted with 200 mL of 0.5M Na2S2O3. The aqueous phase was removed and the organic phase was washed with 200 mL of brine. The organic phase was separated, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by column chromatography (0-30% EtOAc/hexanes) to give tert-butyl 1-bromospiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4′-piperidine]-1′-carboxylate. ESI-MS m/z calc. 418.1. found 419.0 (M+1)+; Retention time: 2.29 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-217b49d0ba914aa1b2d87ab0e8532e4b
Source noteuspto-grants-2013_12