Butylamine → HCID 78322696, compound
Reaction equation
[C:1]1([N:7]2[C:12](=[O:13])[C:11]3[S:14][CH:15]=[C:16]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[C:10]=3[N:9]=[CH:8]2)C=C[CH:4]=[CH:3][CH:2]=1.NC1C(C2C=CC=CC=2)=CSC=1C(OC)=O.C(OCC)(OCC)OCC.C(N)CCC>C(O)(=O)C>[CH2:1]([N:7]1[C:12](=[O:13])[C:11]2[S:14][CH:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:10]=2[N:9]=[CH:8]1)[CH2:2][CH2:3][CH3:4]Participants
6
Procedure
In the same manner as the synthesis of Compound 1, methyl 3-amino-4-phenylthiophene-2-carboxylate (100 mg, 0.43 mmol), triethyl orthoformate (1.0 ml), n-butylamine (0.097 ml, 0.99 mmol), and acetic acid (0.1 ml) were used to give 92 mg (0.32 mmol, 75.2% yield) of the title compound.
Sources & evidence
- ORD record
- ord-c20182222d55455884bfc61c52981354
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09260448B2
Reaction notes
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