Hydrochloric Acid → HCID 86710204, compound
Reaction equation
[ClH:1].[CH3:2][N:3]([CH:11]1[CH2:16][CH2:15][N:14]([C:17]2[C:18]3[C:25]([CH3:26])=[CH:24][NH:23][C:19]=3[N:20]=[CH:21][N:22]=2)[CH2:13][CH2:12]1)C(=O)OC(C)(C)C>O1CCOCC1>[ClH:1].[CH3:2][NH:3][CH:11]1[CH2:16][CH2:15][N:14]([C:17]2[C:18]3[C:25]([CH3:26])=[CH:24][NH:23][C:19]=3[N:20]=[CH:21][N:22]=2)[CH2:13][CH2:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4M HCl in 1,4-Dioxane (6 mL) was added to 1,1-dimethylethyl methyl[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]carbamate D22 (0.793 g) and the mixture stirred for 2 hours. The mixture was filtered under vacuum. The solid was washed with dioxane and Et2O. The white powder was dried under vacuum all the night to give the desired product D23 in 0.6479 g. LCMS [M+H][email protected] min (5 min run)
Workup
- filtrationThe mixture was filtered under vacuum
- washThe solid was washed with dioxane and Et2O
- customThe white powder was dried under vacuum all the night
Sources & evidence
- ORD record
- ord-69639569f53d4001b596bce4d8df25b1
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09045485B2
Reaction notes
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