Hydrochloric Acid → HCID 90411275, compound
Reaction equation
[F:1][C:2]([F:25])([F:24])[C:3]1[N:4]=[CH:5][C:6]([NH:9][C@@H:10]2[CH2:15][C@@H:14]3[N:16](C(OC(C)(C)C)=O)[C@H:11]2[CH2:12][CH2:13]3)=[N:7][CH:8]=1.[ClH:26]>C(Cl)Cl.O1CCOCC1>[ClH:26].[F:25][C:2]([F:1])([F:24])[C:3]1[N:4]=[CH:5][C:6]([NH:9][C@@H:10]2[CH2:15][C@@H:14]3[NH:16][C@H:11]2[CH2:12][CH2:13]3)=[N:7][CH:8]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To the intermediate of Example 181 Step A (100 mg, 0.3 mmol) in DCM (3 mL) was added 4M HCl in dioxane (0.8 mL). The reaction was allowed to proceed overnight then concentrated neutralized with 5% Na2CO3 (aq) and extracted with DCM (2×). The combined organics were dried (Na2SO4) to give the title compound of step A that was used without further purification.
Workup
- concentrationthen concentrated
- extractionextracted with DCM (2×)
- dry with materialThe combined organics were dried (Na2SO4)
Sources & evidence
- ORD record
- ord-1eeccaffa41047baa80d0557300d5d1a
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062078B2
Reaction notes
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