Hydrochloric Acid → HCID 178477948, compound

HRID 1915585Notes

Reaction equation

HRID 1915585 reaction equation
[CH:1]1([C:4]2[N:42]=[C:7]3[N:8]=[C:9]([C:18]4[CH:23]=[CH:22][C:21]([CH2:24][N:25]5[CH2:30][CH2:29][CH:28]([C:31]6[N:35]=[C:34]([C:36]7[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=7)[NH:33][N:32]=6)[CH2:27][CH2:26]5)=[CH:20][CH:19]=4)[C:10]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)=[CH:11][N:6]3[N:5]=2)[CH2:3][CH2:2]1.[ClH:43]>CO>[ClH:43].[CH:1]1([C:4]2[N:42]=[C:7]3[N:8]=[C:9]([C:18]4[CH:19]=[CH:20][C:21]([CH2:24][N:25]5[CH2:26][CH2:27][CH:28]([C:31]6[N:35]=[C:34]([C:36]7[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=7)[NH:33][N:32]=6)[CH2:29][CH2:30]5)=[CH:22][CH:23]=4)[C:10]([C:12]4[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=4)=[CH:11][N:6]3[N:5]=2)[CH2:2][CH2:3]1

Participants

4

Procedure

To 8.08 g 2-Cyclopropyl-6-phenyl-5-(4-{[4-(5-pyridin-2-yl-1H-1,2,4-triazol-3-yl)piperidin-1-yl]methyl}phenyl)[1,2,4]triazolo[1,5-a]pyrimidine (prepared as described under example 4) in 77 ml methanol are added 2.50 ml hydrochloride solution (5.84N in methanol). The mixture is stirred at room temperature for 1 h. The solvent is removed to yield the desired product.

Workup

  1. customThe solvent is removed

Sources & evidence

ORD record
ord-00b635fe26b24c7eae0333991a927e94
Source dataset
uspto-grants-2013_12
Patent number
US08614218B2

Reaction notes

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