2,3-Dihydro-1-benzofuran-7-amine → (S)-2-Amino-6-(5-(2,3-dihydrobenzofuran-7-ylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-one
Reaction equation
COC1C=CC(C([NH:24][C:25]2[N:30]([CH3:31])[C:29](=[O:32])[C:28]([CH3:34])([CH3:33])[C@:27]([C:36]3[CH:41]=[C:40](Br)[CH:39]=[CH:38][C:37]=3[F:43])([CH3:35])[N:26]=2)(C2C=CC(OC)=CC=2)C2C=CC=CC=2)=CC=1.[O:44]1[C:48]2[C:49]([NH2:53])=[CH:50][CH:51]=[CH:52][C:47]=2[CH2:46][CH2:45]1>>[NH2:24][C:25]1[N:30]([CH3:31])[C:29](=[O:32])[C:28]([CH3:34])([CH3:33])[C@:27]([C:36]2[CH:41]=[C:40]([NH:53][C:49]3[C:48]4[O:44][CH2:45][CH2:46][C:47]=4[CH:52]=[CH:51][CH:50]=3)[CH:39]=[CH:38][C:37]=2[F:43])([CH3:35])[N:26]=1Participants
3
Reactant 2
Product 1
Procedure
The coupling of (S)-2-{[bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-6-(5-bromo-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate K) and 2,3-dihydro-benzofuran-7-ylamine according to procedure B followed by deprotection yielded the title compound as an off-white solid. MS (ESI): m/z=397.2 [M+H]+.
Sources & evidence
- ORD record
- ord-44335526e4af441abba12e2c545e90b5
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815881B2
Reaction notes
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