HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230007Generated: November 2, 2026
1,2-Dichloroethane → HCID 178481254, compound
https://huagongshe.com/reaction/230007
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-{[(4-Tert-butylcyclohexyl)(5-hydroxy-1-methyl-1h-benzimidazol-2-yl)amino]methyl}benzoic acid | HCID 68836173 | — |
| Reactant | HCID 178509300 | HCID 178509300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178481254 | HCID 178481254 | — |
Reaction Steps
To a solution of the title compound of Example 15 Step B (0.02 mmol, 10 mg), 1H-tetraazol-5-amine monohydrate (0.2 mmol, 21 mg), HOBt (0.2 mmol, 31 mg) and DIEA (0.3 mmol, 52 μL) in 0.5 mL of DMF was added EDC (0.2 mmol, 38 mg). The reaction was heated to 40° C. 15 min, then allowed to stand at ambient temperature overnight. The reaction mixture was concentrated under reduced pressure. The residue was taken up in ca. 2:1 dioxane/H2O and acidified with TFA, then purified by reverse-phase chromatography (Condition B). The product was lyophilized affording the title compound as a white solid. MS (ESI): m/z 503 (M+H). HPLC A: 1.88 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563815B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-27b2d7bd8e024422a541cee6563365ea |
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| Source note | uspto-grants-2009_07 |
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