Hydrogen Bromide → HCID 18762647, compound
Reaction equation
C(OC(=O)[N:10]([CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[NH:26][CH:27]=[O:28])[CH:11]1[CH2:16][CH2:15][C:14](=[O:17])[NH:13][C:12]1=[O:18])C1C=CC=CC=1.Br>C(O)(=O)C>[O:18]=[C:12]1[CH:11]([NH:10][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[NH:26][CH:27]=[O:28])[CH2:16][CH2:15][C:14](=[O:17])[NH:13]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.00 g of the product from stage 1 was reacted as described in Example 1, stage 5, with 3 ml of hydrobromic acid in acetic acid (33% HBr). After similar working-up, 0.79 g (91% of theory) of the title compound was obtained in the form of a yellowish solid, which was reacted further without purification.
Sources & evidence
- ORD record
- ord-380469d9b45547f9a8d91bccc637f23b
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183274B2
Reaction notes
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