反応式
[NH2:1][C:2]1[N:11]=[C:10]([NH2:12])[C:9]2[C:4](=[N:5][CH:6]=[C:7]([CH2:13]O)[N:8]=2)[N:3]=1.[OH:15][CH2:16][C:17]([CH2:19]O)=[O:18]>>[CH3:19][C:17]([CH:16]=[O:15])=[O:18].[NH2:1][C:2]1[N:11]=[C:10]([NH2:12])[C:9]2[C:4](=[N:5][CH:6]=[C:7]([CH3:13])[N:8]=2)[N:3]=1参加物
4
実験手順
The main disadvantage in the literature methods for the preparation of 2,4-diamino-6-hydroxymethylpteridine is the necessity to use a pure 1,3-dihydroxyacetone, free of methyl-glyoxal, which affords by condensation a considerable yield of 2,4-diamino-6-methylpteridine. Purification of 1,3-dihydroxyacetone is rather difficult, especially the final distillation under high vacuum.
出典と根拠
- ORDレコード
- ord-94d05c2163b04a16b06d1936a2fcb1c4
- 出典データセット
- uspto-grants-1976_11
- 特許番号
- US03989703
関連ノート
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