Hydrochloric Acid → HCID 71268826, compound

HRID 1025381Notes

Reaction equation

HRID 1025381 reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:12]=[C:13]([NH:22][C:23]3[CH:42]=[CH:41][C:26]([CH2:27][N:28]4[CH2:33][CH2:32][N:31](C(OC(C)(C)C)=O)[CH2:30][CH2:29]4)=[CH:25][CH:24]=3)[C:14]3[C:19](=[O:20])[NH:18][N:17]=[CH:16][C:15]=3[N:21]=2)=[CH:7][CH:6]=1)=[O:4].[ClH:43]>O1CCOCC1>[ClH:43].[O:20]=[C:19]1[NH:18][N:17]=[CH:16][C:15]2[N:21]=[C:11]([C:8]3[CH:7]=[CH:6][C:5]([C:3]([O:2][CH3:1])=[O:4])=[CH:10][CH:9]=3)[N:12]=[C:13]([NH:22][C:23]3[CH:24]=[CH:25][C:26]([CH2:27][N:28]4[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]4)=[CH:41][CH:42]=3)[C:14]1=2

Participants

4

Procedure

Tert-butyl 4-(4-(2-(4-(methoxycarbonyl)phenyl)-5-oxo-5,6-dihydropyrimido[4,5-d]pyridazin-4-ylamino)benzyl)piperazine-1-carboxylate (0.1 g, 0.175 mmol) was dissolved in dioxane.HCl (5 mL) and stirred at room temperature for 1.5 hours. The solid obtained was filtered and the residue washed with EtOAc and dried to give the desired product (40 mg).

Workup

  1. customThe solid obtained
  2. filtrationwas filtered
  3. washthe residue washed with EtOAc
  4. customdried

Sources & evidence

ORD record
ord-5e3464f08dde481295e64c21f209fb37
Source dataset
uspto-grants-2014_05
Patent number
US08729079B2

Reaction notes

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