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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394991Generated: October 26, 2026

Mibefradil dihydrochloride → HCID 9830209, compound

https://huagongshe.com/reaction/2394991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMibefradil dihydrochlorideHCID 60662—
ReactantMibefradilHCID 60663—
ReactantDiisopropylethylamineHCID 81531—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
Reactant2-(3-(methylamino)propyl)-1H-benzimidazoleHCID 3145400—
ReactantCalciumHCID 5460341—
ReactantHCID 86657121HCID 86657121—
ProductHCID 9830209HCID 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 antihypertensive POSICOR®. 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 to form mibefradil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811556
Source datasetuspto-grants-1998_09
ORD IDord-458a637f305a41d791d860595f7878d2
Source noteuspto-grants-1998_09