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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63895Generated: October 31, 2026

N-bromobutanimide → 6-bromo-3-(3-(tert-butyldimethylsilyloxy)propyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/63895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 131737211HCID 131737211—
SolventDichloromethaneHCID 6344—
Product6-bromo-3-(3-(tert-butyldimethylsilyloxy)propyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 13173721093.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(3-(tert-butyldimethylsilyloxy)propyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (3.0 g, 8.14 mmol) in DCM (30 mL) at 0° C. was added NBS (1.6 g, 8.95 mmol). The reaction was stirred at 0° C. for 2 h then diluted with DCM (100 mL) and washed with water (2×50 mL). The organic layer was dried over Na2SO4 and concentrated to a residue which was purified by chromatography PE/EA (1:1) to give 6-bromo-3-(3-(tert-butyldimethylsilyloxy) propyl)-1,5-dimethylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (3.4 g, 93.4% yield) as a white solid. LCMS: MH+ 448 and TR=2.917 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447114B2
Source datasetuspto-grants-2016_09
ORD IDord-054afdd1e7bd4dffb3d686dd86de7f5d
Source noteuspto-grants-2016_09