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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397490Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-(Azidomethyl)-1H-1,3-benzodiazole

https://huagongshe.com/reaction/397490

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-(Hydroxymethyl)-1H-benzimidazoleHCID 13505556—
SolventTetrahydrofuranHCID 8028—
Product5-(Azidomethyl)-1H-1,3-benzodiazoleHCID 23000173—

Reaction Steps

To a cooled (0° C.) suspension of 5-(hydroxymethyl)-benzimidazole (920 mg, 6.2 mmol) in THF (12 mL) was added sequentially DPPA (1.46 mL, 6.8 mmol) and DBU (1.11 mL, 7.4 mmol). The resulting solution was heated to reflux for 5 h, cooled to RT, and concentrated in vacuo. The residue was partitioned between sodium bicarbonate and ethyl acetate. The organic layer was washed with brine, dried (Na2SO4), and concentrated in vacuo. Silica gel chromatography (15% MeOH—CHCl3), afforded the title compound as a brown solid: Rf (8:1:1 EtOAc-MeOH—NH4H)=0.31; m.p. 110-114° C.; 1H NMR (400 MHz, DMSO-d6): δ8.25 (s, 1H), 7.27 (d, J=8.4, 1H), 7.62-7.60 (m, 2H), 7.20 (d, J=8.2 Hz, 1H), 8.24 (s, 1H); HRMS (FAB) C8H8N5 calcd. 174.1847 (M+1). Found 174.1222.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610701B2
Source datasetuspto-grants-2003_08
ORD IDord-c08cae394226432fbd6efad8e8611001
Source noteuspto-grants-2003_08