Azide → HCID 22630141, compound
Reaction equation
[N-]=[N+]=[N-].[ClH:4].[CH2:5]([C:8]1([NH2:18])[CH2:13][C:12]([CH3:15])([CH3:14])[CH2:11][C:10](C)([CH3:16])[CH2:9]1)C=C>>[ClH:4].[CH3:5][C:8]1([NH2:18])[CH2:13][C:12]([CH3:15])([CH3:14])[CH2:11][C:10]([CH3:16])=[CH:9]1Participants
3
Procedure
Prepared from azide 39 according to the procedure for compound 11 (Example 3, c). Amine hydrochloride 40 obtained as a colorless solid with 60% yield. 1H NMR (CDCl3, TMS): 0.96 and 1.07 (total 6H, both s, 5,5-CH3); 1.56 (3H, s, 1-CH3); 1.73 (3H, s, 3-CH3); 1.60-2.05 (4H, m, 4,6-CH2); 5.49 (1H, s, C═CH) and 8.27 ppm (3H, br s, NH3+).
Sources & evidence
- ORD record
- ord-43cd12063aa94d9f8bce29ac188d5e25
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06828462B2
Reaction notes
Loading…