Hydrochloric Acid → 5-Phenylethynyl-pyridin-3-ylamine dihydrochloride
Reaction equation
C(OC(=O)[NH:7][C:8]1[CH:9]=[N:10][CH:11]=[C:12]([C:14]#[C:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:13]=1)(C)(C)C.[ClH:23]>O1CCOCC1>[ClH:23].[ClH:23].[C:16]1([C:15]#[C:14][C:12]2[CH:13]=[C:8]([NH2:7])[CH:9]=[N:10][CH:11]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepare essentially as described in EXAMPLE 2 from 5-phenylethynyl-pyridin-3-yl)-carbamic acid tert-butyl ester, (prepared as described in EXAMPLE 154), (0.380 g, 1.3 mmol) in 1,4-dioxane (1 mL) and hydrogen chloride (3 mL, 12 mmol) to give the title compound (280 mg, 81%).
Workup
- customPrepare essentially
Sources & evidence
- ORD record
- ord-a57a3929e4f14f7da9009757dc40441e
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07915424B2
Reaction notes
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