Hydroxylamine → HCID 10086467、化合物
反応式
[NH2:1][C:2]1[N:7]=[C:6](Cl)[C:5]([CH2:9][C:10]2[CH:15]=[C:14]([O:16][CH3:17])[C:13]([O:18][CH3:19])=[C:12]([O:20][CH3:21])[CH:11]=2)=[CH:4][N:3]=1.[NH2:22][OH:23].Cl.NO.[Na]>CO>[NH2:1][C:2]1[N:7]=[C:6]([NH:22][OH:23])[C:5]([CH2:9][C:10]2[CH:15]=[C:14]([O:16][CH3:17])[C:13]([O:18][CH3:19])=[C:12]([O:20][CH3:21])[CH:11]=2)=[CH:4][N:3]=1参加物
6
実験手順
3 g of 2-amino-4-chloro-5-(3,4,5-trimethoxybenzyl)-pyrimidine is added to a methanolic hydroxylamine solution prepared from 1.4 g of hydroxylamine-hydrochloride, 0.46 g of sodium and 50 ml of absolute methanol. The mixture is stirred for 48 hours at 40°; it is subsequently concentrated in vacuo and the residue is recrystallised from butanol to obtain 2-amino-4-(hydroxyamino)-5-(3,4,5-trimethoxybenzyl)-pyrimidine, M.P. 208°-210°, which is identical to the product described in Example 2.
後処理
- concentrationit is subsequently concentrated in vacuo
- customthe residue is recrystallised from butanol
出典と根拠
- ORDレコード
- ord-20a760ca266344d3836b3ee248a0be4b
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03947441
反応ノート
読み込み中…