4-Nitrobenzenesulfonyl chloride → HCID 12071413、化合物

HRID 1584564ノート

反応式

HRID 1584564 の反応式
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][C@H:3]([C:11]([OH:13])=[O:12])[NH:2]1.[OH-].[Na+].C(Cl)Cl.O.[N+:20]([C:23]1[CH:28]=[CH:27][C:26]([S:29](Cl)(=[O:31])=[O:30])=[CH:25][CH:24]=1)([O-:22])=[O:21]>C(Cl)Cl.C(Cl)(Cl)Cl.Cl>[N+:20]([C:23]1[CH:24]=[CH:25][C:26]([S:29]([N:2]2[C@@H:3]([C:11]([OH:13])=[O:12])[CH2:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH2:1]2)(=[O:31])=[O:30])=[CH:27][CH:28]=1)([O-:22])=[O:21]

参加物

8

反応物 4

HCID 74044-Nitrobenzenesulfonyl chloride2 回HCID 14798Sodium Hydroxide2 回HCID 712398(3R)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acidHCID 21908982Water methylene chloride

生成物 1

HCID 12071413HCID 12071413、化合物収率 37%

試薬・触媒・溶媒 3

HCID 313Hydrochloric Acid溶媒HCID 6212Chloroform溶媒HCID 6344Dichloromethane溶媒2 回

実験手順

(3R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid (5.32 g) and sodium hydroxide (2.40 g) are added to a mixture of methylene chloride-water (200 ml--200 ml), and thereto is added dropwise a solution of 4-nitrophenylsulfonyl chloride (6.62 g) in methylene chloride (100 ml) under ice cooling over a period of 30 minutes. The mixture is stirred under ice cooling for 3 hours, and thereto are further added sodium hydroxide (1.20 g) and a solution of 4-nitrophenylsulfonyl chloride (3.32 g) in methylene chloride (60 ml) in this order. The mixture is stirred under ice cooling for 2 hours, and further stirred at room temperature for 17 hours, and the reaction mixture is diluted with chloroform and 10% hydrochloric acid. The chloroform layer is collected and washed with water and then with an aqueous saturated saline solution, dried over sodium sulfate and then treated with active carbon. Undissolved materials are filtered off from the chloroform layer, and the solvent is distilled off under reduced pressure. The residue is purified with a silica gel column chromatography (eluent, chloroform) and recrystallized from ethyl acetate-hexane to give (3R)-N-(4-nitrophenylsulfonyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (4.01 g) as colorless crystals.

後処理

  1. stirringThe mixture is stirred under ice cooling for 2 hours
  2. stirringfurther stirred at room temperature for 17 hours
  3. customThe chloroform layer is collected
  4. washwashed with water
  5. dry with materialwith an aqueous saturated saline solution, dried over sodium sulfate
  6. additiontreated with active carbon
  7. filtrationUndissolved materials are filtered off from the chloroform layer
  8. distillationthe solvent is distilled off under reduced pressure
  9. customThe residue is purified with a silica gel column chromatography (eluent, chloroform)
  10. customrecrystallized from ethyl acetate-hexane

出典と根拠

ORDレコード
ord-afe92d3c771a4476bc7c2702a096b583
出典データセット
uspto-grants-1999_08
特許番号
US05932732

反応ノート

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