Methanol → HCID 57779708, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:27])[CH:4]([CH:11]1[CH2:16][CH2:15][N:14](C(OCC2C=CC=CC=2)=O)[CH2:13][CH2:12]1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.CO>CCO>[C:5]1([CH:4]([CH:11]2[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)[C:3]([O:2][CH3:1])=[O:27])[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the same procedure as described in Example 10, step 1, but substituting 2-nitro-4-(thiophen-2-yl)aniline for compound 91, and MeOH for EtOH, the title compound 92 (0.384 g, 99%) was obtained as a colorless oil. LRMS (ESI): (calc) 233.31 (found) 234.14 (MH)+
Sources & evidence
- ORD record
- ord-61eca603e397404693d67e1e73245167
- Source dataset
- uspto-grants-2015_08
- Patent number
- US09096565B2
Reaction notes
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