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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636849Generated: October 29, 2026

Allyl bromide → HCID 12016520, compound

https://huagongshe.com/reaction/1636849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 12016519HCID 12016519—
SolventDimethylformamideHCID 6228—
ProductHCID 12016520HCID 12016520—

Reaction Steps

A 50 mg portion of 6-amino-5-chloro-2-(4-methyl-1-piperazinyl)benzoxazole was dissolved in 5 ml of DMF, and the solution, while stirring at room temperature, was mixed with 135 mg of allyl bromide and stirred for additional 2 hours. Thereafter, the solvent was evaporated under a reduced pressure and the thus obtained mixture was purified by an LH-20 gel column chromatography (chloroform:methanol=1:1) to obtain the title compound (15 mg) in light yellow color. 1H-NMR (CD3OD) δ values: 3.17 (3 H, s), 3.5-3.7 (4 H, m), 3.8-4.2 (4 H, m), 4.13 (2 H, d), 5.65-5.8 (2 H, m), 6.0-6.15 (1 H, m), 6.93 (1 H, s), 7.20 (1 H, s); MS (EI): m/z 306 (M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06037342
Source datasetuspto-grants-2000_03
ORD IDord-9163e62f918546c6a65dffe83a0c16f1
Source noteuspto-grants-2000_03