HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872768Generated: November 3, 2026
1-Hydroxybenzotriazole → HCID 86755696, compound
https://huagongshe.com/reaction/1872768
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-Methyl-1-benzofuran-2-carboxylic acid | HCID 600591 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 86755697 | HCID 86755697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86755696 | HCID 86755696 | 45.2% |
Reaction Steps
3-methyl-2-benzofurancarboxylic acid (0.100 g) and 1-hydroxy-1H-benzotriazole (0.070 g) were added to (±)-trans-1-[(2-methyl-5-oxazolyl)methyl]-N-[1-[2-(phenylmethyl)-4-piperidinyl]-4-piperidinyl]-1H-benzimidazol-2-amine (0.100 g) in CH2Cl2 (5 ml). The mixture was stirred under N2 atmosphere. A solution of triethylamine (0.5 ml) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1:1) (0.080 g) in CH2Cl2 (10 ml) was added dropwise and the reaction mixture was stirred overnight at RT, under N2. Then, the compound was isolated and purified by column chromatography (eluent gradient: (0.5% ammoniumacetate in H2O)/CH3OH/CH3CN 70/15/15 upgrading over 0/50/50 to 0/0/100). The desired fractions were collected and the solvent was evaporated, yielding 0.060 g of (±)-trans-1-[(3-methyl-2-benzofuranyl)-carbonyl]-4-[4-[[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]-2-(phenylmethyl)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06110939 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-940d9e79793a41cd8b8e395babffb459 |
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| Source note | uspto-grants-2000_08 |
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