Iodoethane → HCID 10019865, compound

HRID 743059Notes

Reaction equation

HRID 743059 reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([N:7]2[CH:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[NH:9][C:8]2=[O:23])[CH2:3][CH2:2]1.[CH2:24](I)[CH3:25]>>[CH2:24]([N:1]1[CH2:2][CH2:3][CH:4]([N:7]2[CH:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[NH:9][C:8]2=[O:23])[CH2:5][CH2:6]1)[CH3:25]

Participants

3

Reactant 2

HCID 6340IodoethaneHCID 15896329HCID 15896329, compound

Product 1

HCID 10019865HCID 10019865, compound

Procedure

In similar way as in Preparation Example 31, the title compound was synthesized from 3-(piperidin-4-yl)-4-phenyl-3,4-dihydro-2(1H)-quinazolinone and ethyl iodide.

Workup

  1. customIn similar way as in Preparation Example 31

Sources & evidence

ORD record
ord-962741bcb6cd45f49fb9c44dfd63736a
Source dataset
uspto-grants-1996_09
Patent number
US05556860

Reaction notes

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