Ammonia → HCID 178479172, compound
Reaction equation
C(O[C:4]1[C:7](=[O:8])[C:6](=[O:9])[C:5]=1[NH:10][C@H:11]1[CH2:16][CH2:15][C@H:14]([CH2:17][CH2:18][N:19]2[CH2:23][C@H:22]3[C:24]4[CH:25]=[C:26]([C:32]#[N:33])[CH:27]=[CH:28][C:29]=4[O:30][CH2:31][C@@H:21]3[CH2:20]2)[CH2:13][CH2:12]1)C.[NH3:34].[ClH:35]>C(O)C.C(#N)C>[ClH:35].[NH2:34][C:4]1[C:7](=[O:8])[C:6](=[O:9])[C:5]=1[NH:10][C@H:11]1[CH2:16][CH2:15][C@H:14]([CH2:17][CH2:18][N:19]2[CH2:23][C@H:22]3[C:24]4[CH:25]=[C:26]([C:32]#[N:33])[CH:27]=[CH:28][C:29]=4[O:30][CH2:31][C@@H:21]3[CH2:20]2)[CH2:13][CH2:12]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1.17 g of the compound obtained in Step A of Example 20 (2.61 mmol) in 13 ml of ethanol is treated with 13 ml of a saturated solution of ammonia in acetonitrile for 16 hours. The solid obtained is filtered off and then washed with ethyl acetate to finally yield, after converting to a salt in ethanol in the warm state using 1N ethereal HCl, the title product.
Workup
- customThe solid obtained
- filtrationis filtered off
- washwashed with ethyl acetate
- customto finally yield
Sources & evidence
- ORD record
- ord-4fe871cc2d5e4d38ad85e3d2b6e51163
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247441B2
Reaction notes
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