Benzylamine → N-benzyl-N-[thieno[2,3-d]pyrimidin-6-ylmethylidene]amine
Reaction equation
CO[C:3]1[CH:4]=[C:5]([CH:18]=[CH:19][C:20]=1OC)[CH2:6][N:7]=[CH:8][C:9]1[S:17][C:12]2[N:13]=[CH:14][N:15]=[CH:16][C:11]=2[CH:10]=1.C(N)C1C=CC=CC=1>>[CH2:6]([N:7]=[CH:8][C:9]1[S:17][C:12]2[N:13]=[CH:14][N:15]=[CH:16][C:11]=2[CH:10]=1)[C:5]1[CH:4]=[CH:3][CH:20]=[CH:19][CH:18]=1Participants
3
Procedure
The title compound was prepared by a similar process to that described for Intermediate 14 but using benzylamine in place of 3,4-dimethoxybenzylamine. Pale yellow solid (69 mg, 100%), which was used directly without further purification.
Workup
- customPale yellow solid (69 mg, 100%), which was used directly without further purification
Sources & evidence
- ORD record
- ord-380526473e64476f96944287284f4188
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427616B2
Reaction notes
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