Hydrochloric Acid → HCID 59293657, compound
Reaction equation
[C:1]([C:5]1[N:10]=[C:9]([C:11]2[S:15][C:14]([NH:16]C(=O)C)=[N:13][C:12]=2[CH3:20])[CH:8]=[C:7]([CH3:21])[N:6]=1)([CH3:4])([CH3:3])[CH3:2].Cl>>[C:1]([C:5]1[N:10]=[C:9]([C:11]2[S:15][C:14]([NH2:16])=[N:13][C:12]=2[CH3:20])[CH:8]=[C:7]([CH3:21])[N:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound is prepared in analogy to the procedure described in Step 1.2, but using N-[5-(2-tert-butyl-6-methyl-pyrimidin-4-yl)-4-methyl-thiazol-2-yl]-acetamide in place of N-[5-(2-tert-butyl-pyridin-4-yl)-4-methyl-thiazol-2-yl]-acetamide and using 2 N HCl. The reaction mixture is stirred 16 h at RT and then 3 h at 90° C. ESI-MS [M+H]+263.1.
Workup
- custom3 h
- customat 90° C
Sources & evidence
- ORD record
- ord-75fdc23b462f4b2288591c38ee0d75cd
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08227462B2
Reaction notes
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