Hexahydro-1,4-diazepine → HCID 21891616, compound

HRID 720365Notes

Reaction equation

HRID 720365 reaction equation
Cl[CH2:2][C:3]1[O:4][C:5]2[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[C:9]([O:16][CH3:17])=[CH:8][C:6]=2[N:7]=1.[NH:18]1[CH2:24][CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1>>[CH3:17][O:16][C:9]1[C:10]([O:14][CH3:15])=[C:11]([O:12][CH3:13])[C:5]2[O:4][C:3]([CH2:2][N:18]3[CH2:24][CH2:23][CH2:22][N:21]([CH2:2][C:3]4[O:4][C:5]5[C:11]([O:12][CH3:13])=[C:10]([O:14][CH3:15])[C:9]([O:16][CH3:17])=[CH:8][C:6]=5[N:7]=4)[CH2:20][CH2:19]3)=[N:7][C:6]=2[CH:8]=1

Participants

3

Reactant 2

HCID 68163Hexahydro-1,4-diazepineHCID 21891587HCID 21891587, compound

Product 1

HCID 21891616HCID 21891616, compound

Procedure

2-Chloromethyl-5,6,7-trimethoxybenzoxazole (152 mg) and homopiperazine (28 mg) were reacted in the same manner as in Example 1 to obtain the title compound as a free base.

Sources & evidence

ORD record
ord-28ad55b4840e4a16a5fd3a11323b00ed
Source dataset
uspto-grants-2006_11
Patent number
US07135473B2

Reaction notes

Loading…