Azido(trimethyl)stannane → HCID 58754803, compound
Reaction equation
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[C:10]1[CH2:15][CH2:14][C:13]([CH3:17])([CH3:16])[CH2:12][CH:11]=1.[N:18]([Sn:21]([CH3:24])([CH3:23])[CH3:22])=[N+:19]=[N-:20]>>[CH3:16][C:13]1([CH3:17])[CH2:14][CH2:15][C:10]([C:3]2[CH:4]=[C:5]([C:6]3[N:18]([Sn:21]([CH3:24])([CH3:23])[CH3:22])[N:19]=[N:20][N:7]=3)[CH:8]=[CH:9][C:2]=2[NH2:1])=[CH:11][CH2:12]1Participants
3
Procedure
The title compound was prepared from 4-amino-3-(4,4-dimethyl-cyclohex-1-enyl)-benzonitrile (as prepared in the previous step, 245 mg, 1.08 mmol), and azidotrimethylstannane (246 mg, 1.19 mmol) according to the procedure in Example 52, step (c) (363 mg, 78%). Mass spectrum (ESI, m/z): Calcd. for C15H19N5, 270.1 (M-SnMe3+2H), found 270.1.
Sources & evidence
- ORD record
- ord-13dcc7260e7a4cbcba0e92c6103969f0
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790724B2
Reaction notes
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