5-(aminomethyl)-2-methylpyrimidin-4-amine
N,N-dimethyl-formamide dimethyl acetal
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
Conditions | Yield |
---|---|
1.) 80 to 85 deg C, 2.) 90 deg C, 30 min; | 88.5% |
5-(aminomethyl)-2-methylpyrimidin-4-amine
orthoformic acid triethyl ester
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid Heating; | 71% |
pyridine
4-Amino-2-methyl-5-thioformamidomethylpyrimidin
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
4-Amino-2-methyl-5-thioformamidomethylpyrimidin
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
Conditions | Yield |
---|---|
With pyridine |
5-(aminomethyl)-2-methylpyrimidin-4-amine
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2O 2: pyridine View Scheme |
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
3-Mercapto-4-oxopentyl Acetate
Thiamine formate
Conditions | Yield |
---|---|
With formic acid for 0.5h; Ambient temperature; | 89.3% |
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
2-methyl-4-amino-5-formylaminomethylpyrimidine
Conditions | Yield |
---|---|
an der Luft erfolgt; |
3,4-Dihydro-7-methylpyrimido<4,5-d>pyrimidine
3-Mercapto-4-oxopentyl Acetate
Thiamine hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; formic acid 1.) 30 min, RT, 2.) EtOH, 30 min, RT; Yield given. Multistep reaction; |
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