HCID 20335531, compound → HCID 20335506, compound

HRID 1706429Notes

Reaction equation

HRID 1706429 reaction equation
[I-:1].[N:2]1([C:8]2[CH:17]=[CH:16][C:15]3[N+:14]4[CH:18]=[C:19]5[CH:28]=[CH:27][C:26]6[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=6[N:20]5[C:13]=4[CH:12]=[CH:11][C:10]=3[CH:9]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.[CH3:29]N1CCCC1=O.C(OCC)(=O)C>>[I-:1].[CH3:29][C:24]1[CH:23]=[CH:22][C:21]2[N:20]3[C:13]4[CH:12]=[CH:11][C:10]5[CH:9]=[C:8]([N:2]6[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]6)[CH:17]=[CH:16][C:15]=5[N+:14]=4[CH:18]=[C:19]3[CH:28]=[CH:27][C:26]=2[CH:25]=1

Participants

3

Reactant 2

HCID 20335531HCID 20335531, compoundHCID 66738192HCID 66738192, compound

Product 1

HCID 20335506HCID 20335506, compound

Procedure

3-(1-Piperidinyl)imidazo[1,2-a:3,4-a']diquinolin-15-ium Iodide; dec. at 280° C.-290° C. from N-methyl-2-pyrrolidinone/ethyl acetate.

Workup

  1. customat 280° C.-290° C.

Sources & evidence

ORD record
ord-bcb8b4c3f4b640e3a73df4f34739020b
Source dataset
uspto-grants-1980_06
Patent number
US04207320

Reaction notes

Loading…