Hydrochloric Acid → HCID 58465050, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[S:10][C:11]([NH:36]C(=O)OC(C)(C)C)=[C:12]([C:14](=[O:35])[NH:15][C:16]2[CH:17]=[N:18][N:19]([CH3:34])[C:20]=2[C:21]2[CH2:22][CH2:23][N:24](C(OC(C)(C)C)=O)[CH2:25][CH:26]=2)[N:13]=1.Cl>CO.O1CCOCC1>[NH2:36][C:11]1[S:10][C:9]([C:3]2[C:2]([F:1])=[CH:7][CH:6]=[CH:5][C:4]=2[F:8])=[N:13][C:12]=1[C:14]([NH:15][C:16]1[CH:17]=[N:18][N:19]([CH3:34])[C:20]=1[C:21]1[CH2:22][CH2:23][NH:24][CH2:25][CH:26]=1)=[O:35]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
tert-butyl 2-(2,6-difluorophenyl)-4-(1-methyl-5-(tert-butyloxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-pyrazol-4-ylcarbamoyl)thiazol-5-ylcarbamate (0.10 g, 0.16 mmol) was dissolved in MeOH (3 mL) and HCl in 1,4-dioxane (4.0
Sources & evidence
- ORD record
- ord-626e03f5680d4ec8b9edf44187e2080b
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669361B2
Reaction notes
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