A series of structurally novel 7,8,9,10‐tetrahydropyrido[3′,4′:4,5]pyrrolo[2,3‐c,]quinolines, 4a‐c, were synthesized via a facile Fischer indole cyclization from the appropriately substituted hydrazinoquinolines 2a‐c. Acetamides 4a,c were hydrolyzed to 5a,b and further converted to tertiary amines 6a‐c. Potent antihypertensive activity has been observed with a number of the title compounds as well as the intermediate 3a.