Hydrochloric Acid → Isoquinoline-6-sulfonyl chloride

HRID 1845941ノート

反応式

HRID 1845941 の反応式
N[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N:7][CH:6]=[CH:5]2.N([O-])=O.[Na+].[S:16]([O-:19])([O-])=[O:17].S(=O)(O)[O-].[Na+].S(=O)(=O)(O)O.C(=O)(O)[O-].[Na+].[ClH:35]>[Cu](Cl)Cl.C(O)(=O)C>[Cl:35][S:16]([C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[N:7][CH:6]=[CH:5]2)(=[O:19])=[O:17]

参加物

10

実験手順

4.0 g of 6-aminoisoquinoline (Reference Compound 1) was suspended at 0° C. in 40 mL of concentrated hydrochloric acid (35%). To the suspension, 4.0 g of sodium nitrite was added in small portions, and the mixture was stirred for 30 minutes. This reaction solution was added dropwise at 0° C. to a mixed solution of 20 mL of acetic acid saturated with sulfite gas generated from sodium bisulfite and sulfuric acid, and 298 mg of copper chloride, and the mixture was stirred for 1 hour. The mixture was neutralized by the addition of a saturated aqueous solution of sodium bicarbonate, followed by extraction with dichloromethane (100 mL×2). The organic layer was washed with saturated saline and then dried over anhydrous sodium sulfate. The obtained dichloromethane solution was used in the next reaction without being further purified because the compound of interest was unstable.

後処理

  1. stirringthe mixture was stirred for 1 hour
  2. extractionfollowed by extraction with dichloromethane (100 mL×2)
  3. washThe organic layer was washed with saturated saline
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe obtained dichloromethane solution was used in the next reaction
  6. customwithout being further purified because the compound of interest

出典と根拠

ORDレコード
ord-21efcbfafd874fd48576390005063c52
出典データセット
uspto-grants-2015_02
特許番号
US08951997B2

反応ノート

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