Hydrochloric Acid → HCID 67019495, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:20]=[CH:19][C:8]([CH2:9][NH:10][NH:11]C(OC(C)(C)C)=O)=[CH:7][CH:6]=1)=[O:4].[ClH:21]>>[ClH:21].[NH:10]([CH2:9][C:8]1[CH:19]=[CH:20][C:5]([C:3]([O:2][CH3:1])=[O:4])=[CH:6][CH:7]=1)[NH2:11]Participants
3
Procedure
To the intermediate from step C (1.89 g, 6.75 mmol) was added HCl (4.0 M in dioxane, 100 mL). After stirring the reaction for 16 hours it was concentrated in vacuo to give a white powder. 1H NMR (CD3OD, 500 MHz): 8.09 (d, J=8.0 Hz, 2H), 7.57 (d, J=8.0 Hz, 2H), 4.21 (s, 2H), 3.93 (s, 3H). LC-MS=0.77; (M+H)=181.
Workup
- customthe reaction for 16 hours it
- concentrationwas concentrated in vacuo
- customto give a white powder
Sources & evidence
- ORD record
- ord-88d06e02e46847e7bf82bb3851d964ab
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07649009B2
Reaction notes
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