Azido(trimethyl)stannane → HCID 58754854, 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][CH2:13][CH2:12][CH:11]=1.[N:16]([Sn:19]([CH3:22])([CH3:21])[CH3:20])=[N+:17]=[N-:18]>>[C:10]1([C:3]2[CH:4]=[C:5]([C:6]3[N:16]([Sn:19]([CH3:22])([CH3:21])[CH3:20])[N:17]=[N:18][N:7]=3)[CH:8]=[CH:9][C:2]=2[NH2:1])[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]=1Participants
3
Procedure
The title compound was prepared from 4-amino-3-cyclohex-1-enyl-benzonitrile (as prepared in the previous step, 245 mg, 0.123 mmol) and azidotrimethylstannane (267 mg, 1.29 mmol) according to the procedure in Example 52, step (c) (320 mg, 64%). Mass spectrum (ESI, m/z): Calcd. for C13H15N5, 242.1 (M-SnMe3+2H), found 242.2 (M+H).
Sources & evidence
- ORD record
- ord-42d8e5a4024742a7aaf7b92baf8479c8
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07790724B2
Reaction notes
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