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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591251Generated: November 3, 2026

1,4-Dibromobutane → HCID 19766728, compound

https://huagongshe.com/reaction/1591251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
Reactant6-Methyl-3H-thieno[2,3-d]pyrimidin-4-oneHCID 735018—
SolventDimethylformamideHCID 6228—
ProductHCID 19766728HCID 19766728—

Reaction Steps

To a stirring mixture of NaH (1.7 g, 0.072 mol) in 150 ml anhydrous DMF at room temperature was added 4.0 g (0.024 mol) of 6-methyl thieno[2,3-d]pyrimidin-4(3H)-one (IV-3) and, after the cessation of gas evolution, 20.7 g (0.96 mol) of 1,4-dibromobutane was added. Reaction was complete after 4 days. The solution was concentrated in vacuo, the residue partitioned between CH2Cl2 and water, and the organic phase isolated, dried (MgSO4), and filtered. The filtrate was concentrated and excess dibromobutane removed by Kugelrohr distillation. The solid product residue weighed 4.12 g (57%). The NMR was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206365
Source datasetuspto-grants-1993_04
ORD IDord-5ebed52a02034a88aece6a838d21a4aa
Source noteuspto-grants-1993_04