Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mibefradil | HCID 60663 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 2-(3-(methylamino)propyl)-1H-benzimidazole | HCID 3145400 | — |
| Reactant | Calcium | HCID 5460341 | — |
| Reactant | HCID 86657121 | HCID 86657121 | — |
| Product | HCID 9830209 | HCID 9830209 | — |
Reaction Steps
U.S. Pat. No. 4,808,605 (to Hoffmann-La Roche) discloses various calcium antagonists including mibefradil, (1S,2S)-2-[2-{[3-(1H-benzimidazol-2-yl)propyl]-methylamino}ethyl]-6-fluoro-1-isopropyl-1,2,3,4-tetrahydronaphthalen-2-yl methoxyacetate, the dihydrochloride salt of which is the active ingredient of the antihypertensive Pricor. The synthesis of mibefradil, as described in that patent, involves the reaction of (1S,2S)-6-fluoro-1-isopropyl-2-[2-(4-toluenesulfonyloxy)ethyl]-1,2,3,4-tetrahydronaphthalene-2-ol with [3-(1H-benzimidazol-2-yl)propyl]methylamine in the presence of Hunig base (ethyldiisopropylamine) to form (1S,2S)-2-[2-{[3-(1H-benzimidazol-2-yl)propyl]methylamino }ethyl]-6-fluoro-1-isopropyl-1,2,3,4-tetrahydronaphthalen-2-ol, which is then acylated with methoxyacetyl chloride in chloroform in the presence of ethyidiisopropylamine to form mibefradil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05892055 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-a14a09a70ed04dedb36215ac1ceec960 |
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| Source note | uspto-grants-1999_04 |
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