HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429695Generated: October 30, 2026
1H-Benzotriazole, 1-hydroxy-, ammonium salt (1:1) → HCID 22012581, compound
https://huagongshe.com/reaction/429695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Benzotriazole, 1-hydroxy-, ammonium salt (1:1) | HCID 113175 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 18354839 | HCID 18354839 | — |
| Reactant | HCID 18355157 | HCID 18355157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22012581 | HCID 22012581 | 36% |
Reaction Steps
To a solution of 2methoxy-4-[N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl)carbonylpent-1-yloxy]phenyl]-carbamoyl]benzoic acid (200 mg) in N,N-dimethylformamide (3 ml) at 0° C. were added 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (97 mg), N-hydroxybenzotrizole (79 mg) and 4-amino-2-[(4-methylpiperazin-1-yl)methyl]-1H-benzimidazole (105 mg) and the mixture was stirred at ambient temperature for 15 hours. The reaction mixture was poured into saturated sodium bicarbonate aqueous solution and extracted with chloroform. The organic layer was washed with saturated sodium bicarbonate aqueous solution and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (chloroform:methanol=10:1) to give 3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-methylpiperazin-1-yl) carbonylpent-1-yloxy]-phenyl]-4-[2-[(4-methylpiperazin-1-yl)methyl]-1H-benzimidazol-4-yl]carbamoylbenzamide (104 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316482B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-9bb4e749fec043e38eb219b777168e3c |
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| Source note | uspto-grants-2001_11 |
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