4-Methoxy-2,3-dihydrobenzofuran-3-amine → HCID 178488328, compound
Reaction equation
C([Si]([O:8][CH2:9][C:10]1[C:15]([N+:16]([O-])=O)=[CH:14][CH:13]=[CH:12][C:11]=1[N:19]=[C:20]=S)(C)C)(C)(C)C.[CH3:22][O:23][C:24]1[C:29]2[CH:30]([NH2:33])[CH2:31][O:32][C:28]=2[CH:27]=[CH:26][CH:25]=1>>[CH3:22][O:23][C:24]1[C:29]2[CH:30]([NH:33][C:20]3[O:8][CH2:9][C:10]4[C:15]([NH2:16])=[CH:14][CH:13]=[CH:12][C:11]=4[N:19]=3)[CH2:31][O:32][C:28]=2[CH:27]=[CH:26][CH:25]=1Participants
3
Procedure
The title compound, MS (ISP) m/e=312.0 [(M+H)+], was prepared from tert-butyl-(2-isothiocyanato-6-nitro-benzyloxy)-dimethyl-silane (intermediate 2) and 4-methoxy-2,3-dihydro-benzofuran-3-ylamine according to the procedure described for example 1 and 2.
Sources & evidence
- ORD record
- ord-0d4173c8838a4e5a8978c217e1570fd8
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044047B2
Reaction notes
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