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Acetic Acid → 4-(4-Hydroxymethyl-2-methylanilino)-6,7-dimethoxy-3-quinolinecarboxamide

HRID 1822857
ノート
印刷プレビュー

反応式

HRID 1822857 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][C:7]([C:15]([NH2:17])=[O:16])=[C:6]2[NH:18][C:19]1[CH:24]=[CH:23][C:22]([C:25](OC)=[O:26])=[CH:21][C:20]=1[CH3:29].[BH4-].[Li+].O.C(O)(=O)C>O1CCCC1>[OH:26][CH2:25][C:22]1[CH:23]=[CH:24][C:19]([NH:18][C:6]2[C:5]3[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=3)[N:9]=[CH:8][C:7]=2[C:15]([NH2:17])=[O:16])=[C:20]([CH3:29])[CH:21]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 176Acetic Acid2 回HCID 962WaterHCID 4148881Lithium borohydride2 回HCID 22170299HCID 22170299、化合物

生成物 1

HCID 221702424-(4-Hydroxymethyl-2-methylanilino)-6,7-dimethoxy-3-quinolinecarboxamide収率 43.5%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

6,7-Dimethoxy-4-(4-methoxycarbonyl-2-methylanilino)-3-quinolinecarboxamide (0.080 g, 0.20 mmol) was dissolved in tetrahydrofuran (25 ml, dried over 4 A molecular sieves). Lithium borohydride (0.15 mg, 6.8 mmol) was added. The mixture was stirred for 24 h and additional lithium borohydride (0.050 g, 2.2 mmol) was added. The reaction mixture was stirred for additional 25 h and then poured into a cooled mixture of water (20 ml) and acetic acid (0.5 ml). Acetic acid (2 ml) was added and the mixture was evaporated under reduced pressure. The residue was suspended in water, filtered and the precipitate was washed with water and re-crystallized from aqueous methanol to give the title compound (32 mg, 43%).

後処理

  1. customdried over 4 A molecular sieves)
  2. stirringThe reaction mixture was stirred for additional 25 h
  3. customthe mixture was evaporated under reduced pressure
  4. filtrationfiltered
  5. washthe precipitate was washed with water
  6. customre-crystallized from aqueous methanol

出典と根拠

ORDレコード
ord-db4a0051cd6745c88018d5812e9fbb3b
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07037925B2

反応ノート

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