Methoxyacetyl chloride → HCID 59437484, compound
Reaction equation
[O:1]1[CH:5]=[CH:4][C:3]([C:6]2[N:11]3[N:12]=[C:13]([NH2:15])[N:14]=[C:10]3[CH:9]=[CH:8][CH:7]=2)=[CH:2]1.[CH3:16][O:17][CH2:18][C:19](Cl)=[O:20]>>[O:1]1[CH:5]=[CH:4][C:3]([C:6]2[N:11]3[N:12]=[C:13]([NH:15][C:19](=[O:20])[CH2:18][O:17][CH3:16])[N:14]=[C:10]3[CH:9]=[CH:8][CH:7]=2)=[CH:2]1Participants
3
Procedure
The title compound was prepared following procedure described for intermediate B1, but starting from 5-(3-furyl)[1,2,4]triazolo[1,5-a]pyridin-2-amine ((A2), 660 mg; 0.30 mmol; 1.0 eq.) and methoxyacetyl chloride (65 mg, 0.60 mmol; 2.0 eq.) as a white powder (59 mg, 72%). HPLC, Rt: 2.21 min. (purity 98.2%). LC/MS, M+(ESI): 273.4, M−(ESI): 271.4.
Sources & evidence
- ORD record
- ord-a21701cb80f84e4caf1e58192d83d32d
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263595B2
Reaction notes
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