4-(Bromomethyl)-1,2-difluorobenzene → HCID 178507958, compound
Reaction equation
O.[NH2:2][C:3]1[CH:8]=[C:7]([OH:9])[N:6]=[C:5]([SH:10])[N:4]=1.[F:11][C:12]1[CH:13]=[C:14]([CH:17]=[CH:18][C:19]=1[F:20])[CH2:15]Br>>[NH2:2][C:3]1[N:4]=[C:5]([S:10][CH2:15][C:14]2[CH:17]=[CH:18][C:19]([F:20])=[C:12]([F:11])[CH:13]=2)[N:6]=[C:7]([OH:9])[CH:8]=1Participants
3
Procedure
The subtitle compound was prepared according to the procedure of Example 1 step 1) treating 4-amino-6-hydroxy-2-mercaptopyrimidine monohydrate (2.0 g) with 3,4-difluorobenzyl bromide (2.66 g) to afford the subtitle compound as a white solid. Yield: 3.35 g. 1H NMR. δ(DMSO) 7.54 (1H, m), 7.32 (2H, m), 6.58 (2H, bs), 4.96 (1H, bs), 4.29 (2H, s).
Workup
- customThe subtitle compound was prepared
Sources & evidence
- ORD record
- ord-1fc442742e98418e81a5f146dd517733
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08106063B2
Reaction notes
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