HCID 20646, compound → HCID 21489207, compound

HRID 1974292Notes

Reaction equation

HRID 1974292 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=[O:20])[N:8]3[C:15]4[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=4[NH:13][C:9]3=[N:10]2)=[CH:5][CH:4]=1.Cl[CH2:22][CH2:23][N:24]([CH2:28][CH2:29][CH3:30])[CH2:25][CH2:26][CH3:27]>>[CH2:25]([N:24]([CH2:28][CH2:29][CH3:30])[CH2:23][CH2:22][N:13]1[C:9]2=[N:10][C:11]3[C:6]([C:7](=[O:20])[N:8]2[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]1=2)=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[CH:12]=3)[CH2:26][CH3:27]

Participants

3

Reactant 2

HCID 20646HCID 20646, compoundHCID 178487725HCID 178487725, compound

Product 1

HCID 21489207HCID 21489207, compound

Procedure

6-(2-di(n-Propyl)aminoethyl)-3-methoxybenzimidazo[2,1-b]-quinazolin-12(6H)one is prepared with 3-methoxybenzimidazo[2,1-b]-quinazolin-12(6H)one and 2-chlorodi(n-propyl)aminoethane.

Sources & evidence

ORD record
ord-d9495eab3ed541678c7ea366bc2c56ba
Source dataset
uspto-grants-1976_12
Patent number
US04000275

Reaction notes

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