HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399355Generated: October 29, 2026
1,2-Diiodoethane → N-[1-(2-phenylethyl)-5-iodo-4-ethoxycarbonylpyrazol-3-yl]-N-((2'-(N-triphenylmethyl-(1H-tetrazol-5-yl))-biphenyl-4-yl)methyl]-n-propylamine
https://huagongshe.com/reaction/399355
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Diiodoethane | HCID 12224 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | N-[1-(2-phenylethyl)-4-ethoxycarbonyl-5-bromopyrazol-3-yl]-N-[(2'-(N-triphenylmethyl-(1H-tetrazol-5-yl))biphenyl-4-yl)methyl]-n-propylamine | HCID 22103828 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[1-(2-phenylethyl)-5-iodo-4-ethoxycarbonylpyrazol-3-yl]-N-((2'-(N-triphenylmethyl-(1H-tetrazol-5-yl))-biphenyl-4-yl)methyl]-n-propylamine | HCID 88329917 | — |
Reaction Steps
0.18 ml of 1.6M n-butyl lithium/hexane solution were added to THF solution (10 ml) of 202 mg of N-[1-(2-phenylethyl)-5-bromo-4-ethoxycarbonylpyrazol-3-yl]-N-[(2'-(N-triphenylmethyl-(1H-tetrazol-5-yl))biphenyl-4-yl)methyl]-n-propylamine, while cooling with dry ice-acetone. After stirred for 2 hours, 667 mg of 1,2-diiodoethane were added thereto. After stirred for one hour, the mixture was then stirred at room temperature for further one hour. 10 ml of aqueous ammonium chloride solution were added to the reaction solution, THF was distilled off under reduced pressure, and the resultant was extracted with 50 ml of dichloromethane. After dried over magnesium sulfate, this was subjected to silica gel column chromatography (n-hexane--ethyl acetate=5:1) to obtain 84 mg of the intended compound as a pale red, amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817828 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-f7019a4b2f5d42a7a7558ceef88bf1ba |
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| Source note | uspto-grants-1998_10 |
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