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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513866Generated: October 25, 2026

Hydrochloric Acid → HCID 178432276, compound

https://huagongshe.com/reaction/513866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiphenylmethylidenehydrazineHCID 79304—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant7-fluoro-2-methyl-3H-benzimidazol-5-yl amineHCID 68005307—
Solvent4-MethylmorpholineHCID 7972—
ProductHCID 178432276HCID 178432276—

Reaction Conditions

Temperature100 °C

Reaction Steps

In a separate reaction container, 7-fluoro-2-methyl-3H-benzimidazol-5-yl amine (100 mg, 0.44 mmol), lithium bis(trimethylsilyl) amide (190 mg, 1.1 mmol), and benzophenone hydrazone (94.3 mg, 0.48 mmol) were dissolved in N-methyl-morpholine (0.5 ml) under a nitrogen atmosphere. Then, the prepared solution containing the catalyst was added thereto. After deaeration, this was heated and stirred at 100° C. under a nitrogen atmosphere for two hours. The reaction mixture was cooled to room temperature, and then an aqueous solution of 6 M hydrochloric acid (0.5 ml) was added thereto. The organic layer was isolated, and concentrated under reduced pressure. Thus, crude N-benzhydrylidene-N′-(7-fluoro-2-methyl-1H-benzimidazol-5-yl)-hydrazine was obtained. The obtained crude product was used in subsequent reactions without being purified.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102692B2
Source datasetuspto-grants-2015_08
ORD IDord-153fc8c3594f4a33b3ecfdba3608cf17
Source noteuspto-grants-2015_08