Hydrochloric Acid → HCID 68829620, compound
Reaction equation
[N:1]1([CH2:6][C@H:7]2[CH2:11][CH2:10][C@@H:9]([NH:12][CH2:13][C:14]([N:16]3[CH2:20][CH2:19][CH2:18][C@H:17]3[C:21]#[N:22])=[O:15])[CH2:8]2)[CH:5]=[N:4][CH:3]=[N:2]1.[ClH:23]>CCOC(C)=O>[ClH:23].[N:1]1([CH2:6][C@H:7]2[CH2:11][CH2:10][C@@H:9]([NH:12][CH2:13][C:14]([N:16]3[CH2:20][CH2:19][CH2:18][C@H:17]3[C:21]#[N:22])=[O:15])[CH2:8]2)[CH:5]=[N:4][CH:3]=[N:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of Example 37 (100 mg, 0.30 mmol) in EtOAc (3 ml) was added a saturated solution of dry HCl in EtOAc (2 ml). This solution was stirred at RT for 30 min to result a white precipitate. The product was collected by filtration and dried under vacuum to give 112 mg of the product as a white solid; 1H NMR (D2O, 300 MHz) δ 1.44-1.64 (m, 2H), 1.81-2.06 (m, 2H), 2.11-2.37 (m, 7H), 2.60-2.62 (m, 1H), 3.45-3.77 (m, 4H), 4.18-4.38 (m, 2H), 4.40-4.44 (m, 2H), 8.52 (s, 1H), 9.23 (s, 1H).
Workup
- customto result a white precipitate
- filtrationThe product was collected by filtration
- customdried under vacuum
Sources & evidence
- ORD record
- ord-c4ac5fd28acf4313940e2428a58b9d57
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07538128B2
Reaction notes
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