HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823764Generated: October 30, 2026
Diisopropylethylamine → HCID 178500555, compound
https://huagongshe.com/reaction/1823764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | Methyl 3-carbamoylpropanoate | HCID 12550576 | — |
| Reactant | HCID 178508206 | HCID 178508206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178500555 | HCID 178500555 | — |
Reaction Steps
8.9 mg of succinamic acid methyl ester, 25 mg of 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HBTU) and 12 μl diisopropyl-ethylamine were taken up in 0.4 ml dimethylformamide. Reaction mixture was stirred at room temperature for one hour and 5-(4-[1-imidazolyl]-phenylsulfonyloxy)-1H-benzimidazole-2-ylamine was added in 0.2 ml dimethylformamide. Reaction mixture was then stirred at room temperature for 24 hours. Solvent was evaporated in a Jouan model RC 10.10 centrifuge evaporator and title compound was solubilised in 0.5 ml dimethylsulfoxide for LCMS trigged purification yielding 3.9 mg of N-[5-(4-[1-imidazolyl]-phenylsulfonyloxy)-1H-benzimidazole-2-yl]-succinamic-acid-methyl ester. (LC/MS analysis: retention time=2.70 min., mass spectrum: 470.34, [M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041668B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-ddd8504d542740eaa916fe4b1ce00606 |
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| Source note | uspto-grants-2006_05 |
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