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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661978Generated: October 25, 2026

Water → 4-bromo-7-(4-hydroxy-2,2-dimethylbutanamido)-9H-carbazole-1-carboxamide

https://huagongshe.com/reaction/661978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,2-Dimethyl-4-butyrolactoneHCID 94746—
ReactantTrimethylaluminumHCID 16682925—
Reactant7-amino-4-bromo-9H-carbazole-1-carboxamide hydrobromideHCID 66605719—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-7-(4-hydroxy-2,2-dimethylbutanamido)-9H-carbazole-1-carboxamideHCID 5937501446%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 7-amino-4-bromo-9H-carbazole-1-carboxamide hydrobromide (Example 54-2, 500 mg, 1.299 mmol) and 3,3-dimethyldihydrofuran-2(3H)-one (222 mg, 1.948 mmol) in THF (10 mL) was treated with trimethylaluminum (2 M in toluene, 562 mg, 7.79 mmol) dropwise at rt. The mixture was heated at 50° C. for 1.5 h, cooled to rt and treated with water. The mixture was filtered through Celite and the solids were washed thoroughly with DCM and methanol. The filtrate was washed with water, dried and concentrated, and the residue was purified by column chromatography (eluting with a gradient from DCM to 10% ammonia-methanol-DCM) to provide 4-bromo-7-(4-hydroxy-2,2-dimethylbutanamido)-9H-carbazole-1-carboxamide as a yellow solid (250 mg, 46%). Mass spectrum m/z 418, 420 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-5a000805a5ee4f41902c368f0ec51fda
Source noteuspto-grants-2011_12