5-Fluoroindole → 3-(2-bromoethyl)-5-fluoro-1H-indole
Reaction equation
[Br:1][CH2:2][CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10](OC)[CH:11]=2)[NH:6][CH:5]=1.[F:15]C1C=C2C(=CC=1)NC=C2>>[Br:1][CH2:2][CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([F:15])[CH:11]=2)[NH:6][CH:5]=1Participants
3
Procedure
The title compound was synthesized according to above mentioned procedure for 3-(2-bromoethyl)-5-methoxy-1H-indole, starting with 5-fluoroindole yielding a brown oil which was stored in the freezer. LC-MS conditions B: tR=0.82 min, [M(81Br)+MeCN+H]+=244.07.
Sources & evidence
- ORD record
- ord-8f8a52b730eb475cb6355e44fb91ae6c
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09303023B2
Reaction notes
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