HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588098Generated: October 31, 2026
HCID 15222072, compound → HCID 178440121, compound
https://huagongshe.com/reaction/1588098
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 15222072 | HCID 15222072 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178440121 | HCID 178440121 | — |
Reaction Steps
5-Methoxycarbonyl-4-[4-(2-pyridyl)-piperazin-1-yl]methyl-2-propyl-1-[(2'-(N-trityltetrazol-5-yl)biphen-4-yl)methyl]imidazole (1.72 g, 2.10 mmol), obtained from Part B of Example 101, was stirred in 75 mL methanol at reflux for 2 hours. After evaporation of solvent under reduced pressure, the residue was stirred in 30 mL of 1:1 methanol/5% aqueous NaHCO3 for 6 h. The reaction mixture was extracted with 4×50 mL ethyl ether, and the residual organic solvent in the aqueous layer was evaporated under reduced pressure. The product was precipitated by adjusting the pH to 5 with aqueous HCl. The title compound (1.02 g, 84.2%) was collected as a white powder after filtering and drying in vacuo at 60° C. 1H NMR (300 MHz, CDCl3): δ0.86 (t, J=7.3 Hz, 3H); 1.61 (m, 2H); 2.54 (t, J=7.7 Hz, 2H); 2.76 (br s, 4H, piperazine); 3.54 (br s, 4H, piperazine); 3.63 (s, 3H); 3.88 (s, 2H); 5.27 (s, 2H); 6.57-8.13 (m, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05219856 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-67c8c1b7ccbb4a10b02bc4b42e9b59db |
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| Source note | uspto-grants-1993_06 |
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