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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394989Generated: October 26, 2026

Mibefradil Dihydrochloride → HCID 9830209, compound

https://huagongshe.com/reaction/2394989

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 Hoffinann-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 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 in chloroform in the presence of ethyldiisopropylamine to form mibefradil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811557
Source datasetuspto-grants-1998_09
ORD IDord-9f4810356081454aa5a137b7c87827f1
Source noteuspto-grants-1998_09