Hydrochloric Acid → HCID 136401843, compound
Reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][C@@H:12]([NH:30]C(=O)OC(C)(C)C)[C:13](=[O:29])[NH:14][C:15]1[CH:16]=[C:17]2[C:27](=[O:28])[NH:26][N:25]=[CH:24][C:19]3=[CH:20][NH:21][C:22]([CH:23]=1)=[C:18]23.[ClH:38]>O1CCOCC1>[ClH:38].[NH2:30][C@H:12]([CH2:11][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH:1]=1)[C:13]([NH:14][C:15]1[CH:16]=[C:17]2[C:27](=[O:28])[NH:26][N:25]=[CH:24][C:19]3=[CH:20][NH:21][C:22]([CH:23]=1)=[C:18]23)=[O:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Preparation of example 179 from the title compound of Example 158 (57 mg, 0.115 mmol) and 4M HCl in dioxane (10 mL) was carried out analogously to Example 91. Isolation, also in an analogous manner afforded the title compound (48 mg, 0.111 mmol) as an orange/yellow powder in 97% yield.
Sources & evidence
- ORD record
- ord-440146f661244fe281defdd7834d1516
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132533B2
Reaction notes
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