HCID 20042526, compound → HCID 20042530, compound
Reaction equation
[NH2:1][C:2]1[C:7]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([O:16]COC)[CH:11]=2)=[CH:6][CH:5]=[CH:4][N:3]=1>S(=O)(=O)(O)O>[NH2:1][C:2]1[C:7]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([OH:16])[CH:11]=2)=[CH:6][CH:5]=[CH:4][N:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-amino-3-(3-methoxymethoxybenzyloxy)pyridine (7.6 g) and 10% sulfuric acid (150 ml) was stirred at room temperature for 4 hours and the resulting precipitates were collected by filtration. The obtained sulfate was treated with an aqueous solution of sodium bicarbonate and the precipitates were collected by filtration, washed with water, and air-dried to give 2-amino-3-(3-hydroxybenzyloxy)pyridine (4.88 g).
Workup
- customthe resulting precipitates
- filtrationwere collected by filtration
- additionThe obtained sulfate was treated with an aqueous solution of sodium bicarbonate
- filtrationthe precipitates were collected by filtration
- washwashed with water
- customair-dried
Sources & evidence
- ORD record
- ord-5dbd55d9cf1c455497ab466ab3319f56
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04831041
Reaction notes
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