Potassium Carbonate → HCID 178424569, compound
Reaction equation
[N:1]1[C:9]([S:10][CH2:11][C:12]2[O:13][C:14](=[O:28])[C:15]3[C:20]([C:21]=2[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[CH:19][CH:18]=[CH:17][CH:16]=3)=[C:8]2[C:4]([NH:5][CH:6]=[N:7]2)=[N:3][CH:2]=1.Br[CH2:30]C1OC(=O)C2C(C=1C1C=C(C)C=CC=1)=CC=CC=2.O.N1C(S)=C2C(NC=N2)=NC=1.C([O-])([O-])=O.[K+].[K+]>>[N:1]1[C:9]([S:10][CH2:11][C:12]2[O:13][C:14](=[O:28])[C:15]3[C:20]([C:21]=2[C:22]2[CH:23]=[C:24]([CH3:30])[CH:25]=[CH:26][CH:27]=2)=[CH:19][CH:18]=[CH:17][CH:16]=3)=[C:8]2[C:4]([NH:5][CH:6]=[N:7]2)=[N:3][CH:2]=1Participants
5
Procedure
The title compound was made in a similar way as that of the compound of example 10, 3-(bromomethyl)-4-m-tolyl-1H-isochromen-1-one (intermediate C3, 64 mg, 0.194 mmol), 9H-purine-6-thiol hydrate (33 mg, 0.194 mmol) and K2CO3 (27 mg, 0.111 mmol) to give the title compound (64 mg, 82%).
Sources & evidence
- ORD record
- ord-3bd7b97576234aa18bddc6f27e628632
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321776B2
Reaction notes
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