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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710521Generated: October 29, 2026

1H-benzimidazole-5-carbohydrazide → HCID 178492804, compound

https://huagongshe.com/reaction/710521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-benzimidazole-5-carbohydrazideHCID 16637119—
ReactantHCID 178492809HCID 178492809—
ProductHCID 178492804HCID 178492804—

Reaction Steps

The compound was synthesized starting from benzimidazol-5-carbohydrazide (176 mg, 1 mmol) and 3,4-dimethoxyphenylsulfonylthioacetic acid (261 mg; 1 mmol) as described in method 2 but purified by flash chromatography on silica using a CHCl3/MeOH gradient; yield: 0.022 g (5.5%); MS m/z: 401.2 [M+H]+; 1H-NMR (DMSO d6, 400 MHz): δ 3.75 (s, 3H); 3.82 (s, 3H); 5.29 (s, 2H); 7.15 (d, 1H3J=8.7 Hz); 7.328-7.333 (m, 1H); 7.38 (dd, 1H, 4J=2.1 Hz, 3J=8.7 Hz); 7.68-7.72 (m, 1H); 7.78-7.82 (m, 1H); 8.01 (br s, 1H); 8.38 (s, 1H); 12.80 (br s, 1H); HPLC (METHOD [A]): rt 10.19 min (90.6%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181233B2
Source datasetuspto-grants-2015_11
ORD IDord-81fe628556db40a9a54c5a0117afd307
Source noteuspto-grants-2015_11