2-Pyridinemethanamine → HCID 85797591, compound
Reaction equation
[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1.[Cl:9][C:10]1[CH:15]=[CH:14][N:13]=[C:12]2[CH:16]=[C:17]([C:19]([O-])=[O:20])[S:18][C:11]=12.[Li+]>>[N:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[CH2:2][NH:1][C:19]([C:17]1[S:18][C:11]2[C:12](=[N:13][CH:14]=[CH:15][C:10]=2[Cl:9])[CH:16]=1)=[O:20]Participants
3
Procedure
The title compound was prepared from 2-aminomethylpyridine and lithium 7-chloro-thieno[3,2-b]pyridine-2-carboxylate by a procedure analogous to Example 1B. MS: 304/306 (MH+); HPLC Rf: 4.36 min.; HPLC purity: 97%.
Sources & evidence
- ORD record
- ord-ecc2bdfa264147fb8cc5ae33be4cca56
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06964961B2
Reaction notes
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