HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545461Generated: October 28, 2026
Benzoyl chloride → HCID 11359309, compound
https://huagongshe.com/reaction/545461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 131728274 | HCID 131728274 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11359309 | HCID 11359309 | — |
Reaction Steps
To a mixture of 6-aminomethyl-benzo[b]thiophene-2-carboxylic acid ethyl ester, hydrochloride salt (109 mg, 0.40 mmol), NMM (132 μL, 1.20 mmol) an DMAP (10 mg, 0.08 mmol) in anhydrous THF (5 mL) were added benzoyl chloride (55.7 μL, 0.48 mmol) and DMF (2.0 mL). After the reaction was complete, the reaction mixture was concentrated. To the residue were added MeOH (1 mL) and water (10 mL). The solid formed was filtered, washed with water and dried. This solid residue was dissolved in anhydrous MeOH (5 mL) and hydroxylamine hydrochloride (106 mg, 1.52 mmol) was added, followed by the addition of NaOMe solution (4.37 M in MeOH, 0.70 mL, 3.1 mmol). The mixture was allowed to stir at rt till the reaction was complete. The reaction mixture was concentrated and the residue was dissolved in a minimal amount of water. The obtained solution was acidified with 2N HCl to pH≈8. The solid formed was filtered, washed with water, collected and purified by flash column chromatography to give 6-(benzoylamino-methyl)-benzo[b]thiophene-2-carboxylic acid hydroxyamide as a white solid. 1H NMR (DMSO-d6, 200 MHz) δ 11.44 (brs, 1H), 9.27 (brs, 1H), 9.13 (t, J=6.2 Hz, 1H), 8.00-7.78 (m, 5H), 7.58-7.28 (m, 4H), 4.60 (d, J=5.8 Hz, 2H). MS (EI): cal'd 327.1 (MH+), exp 327.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935724B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-7bdd23973e994c6a84f3bdb24d9403f9 |
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| Source note | uspto-grants-2011_05 |
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