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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154544Generated: October 30, 2026

2-Fluoro-1H-benzimidazole → HCID 86739840, compound

https://huagongshe.com/reaction/1154544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-1H-benzimidazoleHCID 13072095—
ReactantHCID 86739841HCID 86739841—
SolventDimethylformamideHCID 6228—
ProductHCID 86739840HCID 8673984083.3%

Reaction Steps

To a solution of anhydrous 6-amino-2,2-dimethylpenam-3-carboxylic acid toluene-p-sulphonate (171 mg.) in dry DMF was added 2-fluorobenzimidazole (150 mg.) in one portion and the mixture stirred at ambient temperature for 1.5 hours. The mixture was evaporated to dryness under reduced pressure at room temperature and the resulting residue, a mobile oil, was triturated with EtOAc (2×10 ml.) and then dry acetonitrile (2 ml.) whereupon the product crystallised. The solid was filtered and washed with acetonitrile and ether to give 6-(benzimidazol-2-yl)amino-2,2-dimethylpenam-3-carboxylic acid toluene-p-sulphonate (185 mg.), m.p. 181°-183°, having the following n.m.r. spectrum in d6DMSO: 1.49 (s, 3H); 1.62 (s, 3H); 2.29 (s, 3H); 4.39 (s, 1H); 5.54 (br, 1H); 5.68 (d, 1H); 7.0-7.56 (m, 8H); 9.93 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490382
Source datasetuspto-grants-1984_12
ORD IDord-0a439c3766634e39abd8bb2389e77baa
Source noteuspto-grants-1984_12