Morpholine → HCID 90370137, compound
Reaction equation
[CH3:1][C:2]1[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[N:4][CH:3]=1.C1C(=O)N(Br)C(=O)C1.[NH:20]1[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1>>[N:20]1([CH2:1][C:2]2[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[N:4][CH:3]=2)[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1Participants
4
Procedure
By using 3.42 g of methyl 6-methylpyrazine-2-carboxylate and 4.40 g of NBS, a bromination reaction was performed by the method similar to Preparation Example 62. Thereafter, by using 10 mL of morpholine as amine, the reaction similar to Preparation Example 9 was performed, thereby obtaining 987 mg of methyl 6-(morpholin-4-ylmethyl)pyrazine-2-carboxylate.
Workup
- customa bromination reaction
- customwas performed by the method similar to Preparation Example 62
- customthe reaction
- customsimilar to Preparation Example 9
Sources & evidence
- ORD record
- ord-30fb0a6af9c84d4e9cb3e4b9415d4e84
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062032B2
Reaction notes
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