Ethanol → HCID 18507208, compound
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:16]=[CH:15][C:11]3[O:12][CH2:13][O:14][C:10]=3[CH:9]=2)[C:5]([C:17]#[N:18])=[C:4](S(C)(=O)=O)[N:3]=1.C1CCN2C(=NCCC2)CC1.[CH2:34]([OH:36])[CH3:35]>>[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:16]=[CH:15][C:11]3[O:12][CH2:13][O:14][C:10]=3[CH:9]=2)[C:5]([C:17]#[N:18])=[C:4]([O:36][CH2:34][CH3:35])[N:3]=1Participants
4
Procedure
From 2-amino-4-benzo[1,3]dioxol-5-yl-6-methanesulfonyl-pyrimidine-5-carbonitrile, ethanol and DBU in DMB. EI-MS rn/e 2%) 284 (M+, 100), 214 (32).
Sources & evidence
- ORD record
- ord-329d0df32e9b4f278f2e118642f59896
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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