HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352662Generated: November 3, 2026
1-Hydroxybenzotriazole → HCID 9804230, compound
https://huagongshe.com/reaction/1352662
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-Amino-1,2,2,6,6-pentamethylpiperidine | HCID 693792 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-(5,6-dichloro-1H-benzimidazol-2-yl)benzoic acid | HCID 4073119 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9804230 | HCID 9804230 | 22% |
Reaction Steps
A mixture of 5,6-dichloro-2-(4-carboxyphenyl)benzimidazole (0.3 g, 0.9 mmol) prepared as described in Preparation 8, 1-hydroxybenzotriazole (0.145 g, 1.08 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.207 g, 1.08 mmol) in THF (10 ml) was heated at 35–40° C. for 1 h. 1,2,2,6,6,-Pentamethyl-4-aminopiperidine in THF (2 ml) was added dropwise and the reaction was refluxed for 1 h. After cooling to room temperature, the solvent was removed under reduced pressure and the residue was treated with 2N NaOH (5 ml). The solid was filtered, washed with water and dried at 50° C. under vacuum. The solid was suspended in isopropyl alcohol and stirred for half an hour, filtered and dried to give 91 mg of the title compound (yield 22%) as an yellow powder, mp>280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07220769B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-175c97a8914a466f9e126cf341ba6d0f |
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| Source note | uspto-grants-2007_05 |
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