Hydrochloric Acid → HCID 66763954, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][N:11]2[N:14]=[CH:15][C:16]([C:17](=[O:40])[NH:18][C:19]3[CH:24]=[CH:23][CH:22]=[C:21]([CH2:25][NH:26][C:27]4[C:36]5[C:31](=[C:32]([C:37](=[O:39])[NH2:38])[CH:33]=[CH:34][CH:35]=5)[N:30]=[CH:29][N:28]=4)[CH:20]=3)=[C:10]2[CH2:9]1)=O)(C)(C)C.Cl>O1CCOCC1>[N:14]1[N:11]2[CH2:12][CH2:13][NH:8][CH2:9][C:10]2=[C:16]([C:17]([NH:18][C:19]2[CH:20]=[C:21]([CH:22]=[CH:23][CH:24]=2)[CH2:25][NH:26][C:27]2[C:36]3[C:31](=[C:32]([C:37]([NH2:38])=[O:39])[CH:33]=[CH:34][CH:35]=3)[N:30]=[CH:29][N:28]=2)=[O:40])[CH:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
37 mg (0.56 mmol) 3-{3-[(8-Carbamoyl-quinazolin-4-ylamino)-methyl]-phenylcarbamoyl}-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazine-5-carboxylic acid tert-butyl ester were dissolved in 1.5 ml dioxane and 280 μl 4 N HCl in dioxane were added. The mixture was stirred overnight and evaporated to dryness. 30 mg, off-white solid. Product is the hydrochloride salt.
Workup
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-a45a34c8686644f59b0c1acb93eaefc4
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040560B2
Reaction notes
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