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Iodine → Tert-butyl 2-(4-(5-hydroxypicolinoyl)phenoxy)ethyl(methyl)carbamate

HRID 626159
ノート
印刷プレビュー

反応式

HRID 626159 の反応式
II.C(Br)C.Br[C:7]1[CH:24]=[CH:23][C:10]([O:11][CH2:12][CH2:13][N:14]([CH3:22])[C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[CH:9][CH:8]=1.[OH:25][C:26]1[CH:27]=[CH:28][C:29]([C:32](N(OC)C)=[O:33])=[N:30][CH:31]=1>C1COCC1>[OH:25][C:26]1[CH:27]=[CH:28][C:29]([C:32]([C:7]2[CH:24]=[CH:23][C:10]([O:11][CH2:12][CH2:13][N:14]([CH3:22])[C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[CH:9][CH:8]=2)=[O:33])=[N:30][CH:31]=1
参加物反応条件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 807IodineHCID 6332Ethyl BromideHCID 20785720tert-butyl N-[2-(4-bromophenoxy)ethyl]-N-methylcarbamate2 回HCID 866889815-hydroxy-N-methoxy-N-methylpicolinamide

生成物 1

HCID 89656144Tert-butyl 2-(4-(5-hydroxypicolinoyl)phenoxy)ethyl(methyl)carbamate

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
3 回

反応条件

温度
55 °C

実験手順

Mg (3.5 eq) was added to a 3-neck round bottom flask containing 50 mL anhydrous THF. The mixture was heated to 55° C. Iodine chips (2 grains) were added in one lot followed by addition of 0.1 mL ethyl bromide. Tert-butyl 2-(4-bromophenoxy)ethyl(methyl)carbamate (3.0 eq) was dissolved in 30 mL anhydrous THF, 3 mL of this solution was added at once to Mg-THF suspension. The reaction was initiated after 30 min and reflux started. The remaining solution of tert-butyl 2-(4-bromophenoxy)ethyl(methyl)carbamate was added dropwise in such speed that the reaction mixture remained reflux. After addition, the reaction mixture was further reflux for 2 h and cooled to rt. 5-Hydroxy-N-methoxy-N-methylpicolinamide (1.0 eq) in 20 mL THF was added dropwise at rt, stirred for 30 min. at rt., quenched with sat NH4Cl (aq), and extracted with EtOAc. The extract was dried, concentrated, and purified by column chromatography to give the desired product.

後処理

  1. temperaturereflux
  2. temperatureremained reflux
  3. additionAfter addition
  4. temperaturethe reaction mixture was further reflux for 2 h
  5. temperaturecooled to rt
  6. custom, quenched with sat NH4Cl (aq)
  7. extractionextracted with EtOAc
  8. customThe extract was dried
  9. concentrationconcentrated
  10. custompurified by column chromatography

出典と根拠

ORDレコード
ord-26f20a740f204824b018520a262be3c4
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309211B2

反応ノート

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