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Dichloromethane → 3,5-Dichloro-N-(4-fluorobenzyl)-N-(4-((4-fluorobenzylamino)methyl)benzyl)-2-hydroxybenzenesulfonamide

HRID 1889667
ノート
印刷プレビュー

反応式

HRID 1889667 の反応式
[NH2:1][CH2:2][C:3]1[CH:30]=[CH:29][C:6]([CH2:7][N:8]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)[S:9]([C:12]2[CH:17]=[C:16]([Cl:18])[CH:15]=[C:14]([Cl:19])[C:13]=2[OH:20])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C(Cl)Cl.[F:34][C:35]1[CH:42]=[CH:41][C:38]([CH:39]=O)=[CH:37][CH:36]=1.[BH4-].[Na+]>C(O)(C)C>[Cl:19][C:14]1[C:13]([OH:20])=[C:12]([S:9]([N:8]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)[CH2:7][C:6]2[CH:5]=[CH:4][C:3]([CH2:2][NH:1][CH2:39][C:38]3[CH:41]=[CH:42][C:35]([F:34])=[CH:36][CH:37]=3)=[CH:30][CH:29]=2)(=[O:11])=[O:10])[CH:17]=[C:16]([Cl:18])[CH:15]=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 6344DichloromethaneHCID 680234-FluorobenzaldehydeHCID 4311764Sodium borohydrideHCID 58531430N-(4-(Aminomethyl)benzyl)-3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamide

生成物 1

HCID 585314183,5-Dichloro-N-(4-fluorobenzyl)-N-(4-((4-fluorobenzylamino)methyl)benzyl)-2-hydroxybenzenesulfonamide収率 57%

試薬・触媒・溶媒

1
HCID 3776Isopropanol溶媒

実験手順

To a solution of N-(4-(aminomethyl)benzyl)-3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamide (235 mg, 0.50 mmol) in a mixed solvent (10 mL of CH2Cl2 and 2 mL of i-propanol) at rt was added 4-fluorobenzaldehyde (62 mg, 0.50 mmol). The reaction mixture was stirred at rt overnight. The next morning, sodium borohydride (37 mg, 1.00 mmol) was added, and the mixture was stirred at rt for 2 h. The reaction mixture was quenched by adding 3 mL of MeOH and 3 ml of saturated aq NaHCO3. The reaction mixture was extracted with EtOAc (3×50 mL). The combined organic extracts were dried, concentrated and purified by prep HPLC to give the title compound (164 mg, 57%) as a white solid. MS (ESI): 577.0 (M+H)+.

後処理

  1. stirringthe mixture was stirred at rt for 2 h
  2. customThe reaction mixture was quenched
  3. additionby adding 3 mL of MeOH and 3 ml of saturated aq NaHCO3
  4. extractionThe reaction mixture was extracted with EtOAc (3×50 mL)
  5. customThe combined organic extracts were dried
  6. concentrationconcentrated
  7. custompurified by prep HPLC

出典と根拠

ORDレコード
ord-d411041a04ed4ca0bb7f576347a039da
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501992B2

反応ノート

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