1,1-dimethylethyl [6-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]acetate → [6-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]acetic acid hydrochloride

HRID 1514264Notes

Reaction equation

HRID 1514264 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:12]2[O:16][N:15]=[C:14]([C:17]3[C:27]4[CH2:26][CH2:25][N:24]([CH2:28][C:29]([O:31]C(C)(C)C)=[O:30])[CH2:23][CH2:22][C:21]=4[CH:20]=[CH:19][CH:18]=3)[N:13]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH:9]([CH3:11])[CH3:10]>Cl.O1CCOCC1>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([C:12]2[O:16][N:15]=[C:14]([C:17]3[C:27]4[CH2:26][CH2:25][N:24]([CH2:28][C:29]([OH:31])=[O:30])[CH2:23][CH2:22][C:21]=4[CH:20]=[CH:19][CH:18]=3)[N:13]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH:9]([CH3:11])[CH3:10]

Participants

4

Procedure

1,1-Dimethylethyl [6-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]acetate (Preparation 19) (120 mg, 0.241 mmol) was stirred at room temperature for 18 hours in 4M HCl in 1,4-dioxane (20 ml). Evaporation and trituration with diethylether yielded the HCl salt [6-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl]acetic acid hydrochloride (110 mg, 0.216 mmol, 90% yield) as a cream powder. MS (ES) C23H2435ClN3O4 requires 441; found 442 [M+H]+.

Workup

  1. customEvaporation and trituration with diethylether

Sources & evidence

ORD record
ord-c37fb2adc80247bc92b083e876508ce5
Source dataset
uspto-grants-2012_07
Patent number
US08222245B2

Reaction notes

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