Hydrochloric Acid → HCID 86731412, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([NH:15]C(=O)OC(C)(C)C)[C:12]([O:23]COC)=[CH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:27]>C1COCC1>[ClH:27].[NH2:15][C:13]1[CH:14]=[C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[N:10]=[CH:11][C:12]=1[OH:23]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
A mixture of tert-butyl (2-(benzyloxy)-5-(methoxymethoxy)pyridin-4-yl)carbamate (11.0 g) in THF (10 mL) and 6 M hydrochloric acid (30 mL) was stirred at 60° C. for 8 hr. The reaction mixture was cooled to 0° C., and the precipitate was collected by filtration, and washed with hexane. The obtained solid was dried under reduced pressure to give the title compound (5.87 g).
Workup
- temperatureThe reaction mixture was cooled to 0° C.
- filtrationthe precipitate was collected by filtration
- washwashed with hexane
- customThe obtained solid was dried under reduced pressure
Sources & evidence
- ORD record
- ord-e0074edd9c0647e8a001863b75ead532
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133129B2
Reaction notes
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