7-Benzyloxy-4-chloro-6-methoxycinnoline hydrochloride → 4-Chloro-7-hydroxy-6-methoxycinnoline

HRID 7477

反応式

HRID 7477 の反応式
Cl.C([O:9][C:10]1[CH:19]=[C:18]2[C:13]([C:14]([Cl:20])=[CH:15][N:16]=[N:17]2)=[CH:12][C:11]=1[O:21][CH3:22])C1C=CC=CC=1>C(O)(C(F)(F)F)=O>[Cl:20][C:14]1[C:13]2[C:18](=[CH:19][C:10]([OH:9])=[C:11]([O:21][CH3:22])[CH:12]=2)[N:17]=[N:16][CH:15]=1

参加物

3

反応物 1

HCID 219910077-Benzyloxy-4-chloro-6-methoxycinnoline hydrochloride

生成物 1

HCID 1357525234-Chloro-7-hydroxy-6-methoxycinnoline収率 94%

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

The starting material, 4-chloro-7-hydroxy-6-methoxycinnoline was obtained by heating a solution of 7-benzyloxy-4-chloro-6-methoxycinnoline hydrochloride (3.06 g, 9 mmol), (prepared as described for the starting material in Example 6), in TFA (30 ml) at reflux for 5 hours. After evaporation of the solvent, the residue was suspended in water and adjusted to pH7 with saturated aqueous sodium hydrogen carbonate solution. The resulting solid was filtered off, washed with water and ether and dried under vacuum to give 4-chloro-7-hydroxy-6-methoxycinnoline as a yellow solid (1.78 g, 94%).

後処理

  1. custom(prepared
  2. temperatureat reflux for 5 hours
  3. customAfter evaporation of the solvent
  4. filtrationThe resulting solid was filtered off
  5. washwashed with water and ether
  6. customdried under vacuum

出典と根拠

ORDレコード
ord-15a0570011444c2ebe97c407c3807efe
出典データセット
uspto-grants-2006_08
特許番号
US07087602B2

関連ノート

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