Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14950483 | HCID 14950483 | — |
| Product | HCID 15171324 | HCID 15171324 | — |
Reaction Steps
Sodium hydride (115 mg) was added to a solution of 2,6-dimethyl-3-hydroxymethyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]pyridine (1.0 g) in DMF (30 ml) and the mixture was stirred for 10 minutes. Iodomethane (0.3 ml) was added and the mixture was stirred for 18 hours. Water (100 ml) was added and the mixture was extracted with ethyl acetate (2×50 ml). The combined extracts were washed with saturated sodium chloride solution (50 ml) and then dried (MgSO4). The solvent was removed by evaporation and the residue was purified by flash chromatography, eluting with a mixture of methanol and dichloromethane on a gradient from 1:50 v/v to 1:20 v/v, to give 2,6-dimethyl-3-methoxymethyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]pyridine (A) (0.74 g), m.p. 132°-135° C.; NMR (d6 -DMSO/d4 -acetic acid): 2.55(s,6H), 3.2(s,3H), 4.45(s,2H), 5.25(s,2H), 6.8-7.9 (complex m,24H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05130318 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-9e505e35f6724e3ba0a6858ae665ff9d |
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| Source note | uspto-grants-1992_07 |
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