HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614590Generated: November 4, 2026
Potassium Hydroxide → HCID 19771715, compound
https://huagongshe.com/reaction/1614590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19771698 | HCID 19771698 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19771715 | HCID 19771715 | 32.8% |
Reaction Steps
A solution of compound B5 (0.42 g) and potassium hydroxide (0.1 g) in methanol (5 ml) was left to stand for 1 hour. The solvent was removed by evaporation and the residue partitioned between ethyl acetate (20 ml) and water (20 ml). The organic phase was separated, washed with saturated sodium chloride solution (20 ml) and dried (MgSO4) The solvent was removed by evaporation and ether (10 ml) was added to the residue. Insoluble material was removed by filtration and the filtrate was evaporated to give 2-ethyl 5,6,7,8-tetrahydro-4-(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl)-4-yl)methoxy]-1,5-naphthyridine (A5) (0.12 g), as a foam; NMR (d6 -DMSO): 1.15(t,3H), 1.8-1.9(m,2H), 2.5(q,2H), 2.7(t,2H), 3.05-3.15(m,2H), 5.05(s,2H), 6.65(s,1H), 6.8-6.9(m,6H), 7.1(d,2H), 7.2-7.7(complex m,14H), 7.9(dd,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198434 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-188d63d0ecc54059bba29a7a35621b56 |
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| Source note | uspto-grants-1993_03 |
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