3-Oxetanamine → 4-Chloro-7-oxetan-3-yl-7H-pyrrolo[2,3-d]pyrimidine
Reaction equation
Cl[C:2]1[C:7]([CH2:8][CH:9]=O)=[C:6]([Cl:11])[N:5]=[CH:4][N:3]=1.[O:12]1[CH2:15][CH:14]([NH2:16])[CH2:13]1>>[Cl:11][C:6]1[C:7]2[CH:8]=[CH:9][N:16]([CH:14]3[CH2:15][O:12][CH2:13]3)[C:2]=2[N:3]=[CH:4][N:5]=1Participants
3
Procedure
The title compound was prepared according to the method described for Preparation 1 using (4,6-dichloropyrimidin-5-yl)acetaldehyde (Preparation 208) and oxetan-3-amine to afford the title compound as a yellow solid in 67% yield, 2.81 g.
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-da372c854fd145ceb2cc65ad5ec2537d
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846698B2
Reaction notes
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