Methanol → HCID 12985380, compound
Reaction equation
[N:1]([CH:4]1[C:16]2[C:8](=[CH:9][CH:10]=[C:11]3[C:15]=2[N:14]([CH2:17][C@@H:18]([NH:20]C(=O)OCC2C=CC=CC=2)[CH3:19])[N:13]=[CH:12]3)[O:7][CH2:6][CH:5]1Br)=[N+]=[N-].C[OH:33]>[Pd]>[NH2:1][CH:4]1[C:16]2[C:8](=[CH:9][CH:10]=[C:11]3[C:15]=2[N:14]([CH2:17][C@@H:18]([NH2:20])[CH3:19])[N:13]=[CH:12]3)[O:7][CH2:6][CH:5]1[OH:33]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from step B (0.26 g, 0.30 mmol) and Pd/C (10%, 0.026 g) were mixed with methanol (5 mL) and placed under a hydrogen atmosphere for 18 h. The mixture was filtered and evaporated to give a yellowish solid (0.155 g, 96%): mp 84-88° C.; LC/MS (+APCI) m/z 263 (M+H).
Workup
- filtrationThe mixture was filtered
- customevaporated
Sources & evidence
- ORD record
- ord-4f19b10671164383a40aa7aaf38257aa
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06881749B2
Reaction notes
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