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Heptane → CCR3 antagonist 1

HRID 1660697
ノート
印刷プレビュー

反応式

HRID 1660697 の反応式
C([O:3][C:4]([CH2:6][C:7]1[N:8]=[C:9]([SH:12])[S:10][CH:11]=1)=[O:5])C.[OH-].[Na+].[Cl:15][C:16]1[CH:17]=[C:18]([CH:32]=[CH:33][C:34]=1[Cl:35])[CH2:19][N:20]1[CH2:25][CH2:24][O:23][C@@H:22]([CH2:26][NH:27][C:28](=[O:31])[CH2:29]Cl)[CH2:21]1.CCCCCCC>O.C(O)(C)(C)C.COC(C)(C)C>[C:4]([CH2:6][C:7]1[N:8]=[C:9]([S:12][CH2:29][C:28]([NH:27][CH2:26][C@@H:22]2[O:23][CH2:24][CH2:25][N:20]([CH2:19][C:18]3[CH:32]=[CH:33][C:34]([Cl:35])=[C:16]([Cl:15])[CH:17]=3)[CH2:21]2)=[O:31])[S:10][CH:11]=1)([OH:3])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8900HeptaneHCID 14798Sodium HydroxideHCID 57686783(2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}chloroacetamideHCID 178470768HCID 178470768、化合物

生成物 1

HCID 11684581CCR3 antagonist 1

試薬・触媒・溶媒 3

HCID 962Water溶媒2 回
HCID 6386
tert-Butanol
溶媒
HCID 15413tert-Butyl methyl ether溶媒

実験手順

4-Ethoxycarbonylmethyl-2-mercaptothiazole (70.14 g) was dissolved in a mixed solution of water (300 ml) and tert-butanol (250 ml), sodium hydroxide (29.46 g) was added on a water bath, and the mixture was stirred for 1.5 hr. To the reaction mixture was added a solution of (2S)-N-{[4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}chloroacetamide obtained in the above-mentioned 1-1 in tert-butyl methyl ether, and the mixture was stirred at 65° C. for 6 hr. n-Heptane (50 ml) and water (50 ml) were added to the reaction mixture, and the mixture was cooled to room temperature. The reaction mixture was stood still and partitioned, and the aqueous layer was further washed with a mixed solvent of tert-butyl methyl ether (200 ml)/n-heptane (20 ml). 6N Hydrochloric acid (60 ml) was added to the aqueous layer, and the mixture was extracted with ethyl acetate (750 ml) and further extracted twice with a mixed solvent of ethyl acetate (175 ml)/tert-butanol (20 ml). The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give a crude product (181 g) of compound 1-2.

後処理

  1. additionwas added on a water bath
  2. stirringthe mixture was stirred at 65° C. for 6 hr
  3. custompartitioned
  4. washthe aqueous layer was further washed with a mixed solvent of tert-butyl methyl ether (200 ml)/n-heptane (20 ml)
  5. addition6N Hydrochloric acid (60 ml) was added to the aqueous layer
  6. extractionthe mixture was extracted with ethyl acetate (750 ml)
  7. extractionfurther extracted twice with a mixed solvent of ethyl acetate (175 ml)/tert-butanol (20 ml)
  8. dry with materialThe obtained organic layer was dried over anhydrous sodium sulfate
  9. customthe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-00e3972b69d449f6a3869f87fadf1892
出典データセット
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08030303B2

反応ノート

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