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Diethyl Ether → Methyl 3-azido-6-bromo-2-(4-(morpholine-4-carbonyl)phenyl)isonicotinate

HRID 2410748
ノート
印刷プレビュー

反応式

HRID 2410748 の反応式
[NH2:1][C:2]1[C:11]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([N:20]3[CH2:25][CH2:24][O:23][CH2:22][CH2:21]3)=[O:19])=[CH:14][CH:13]=2)=[N:10][C:9]([Br:26])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].N([O-])=O.[Na+].[N-:31]=[N+:32]=[N-].[Na+].C(OCC)C>FC(F)(F)C(O)=O>[N:1]([C:2]1[C:11]([C:12]2[CH:13]=[CH:14][C:15]([C:18]([N:20]3[CH2:21][CH2:22][O:23][CH2:24][CH2:25]3)=[O:19])=[CH:16][CH:17]=2)=[N:10][C:9]([Br:26])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5])=[N+:31]=[N-:32]
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 3283Diethyl EtherHCID 33557Sodium AzideHCID 23668193Sodium NitriteHCID 86663019Methyl 3-amino-6-bromo-2-(4-(morpholine-4-carbonyl)phenyl)isonicotinate

生成物 1

HCID 86663020Methyl 3-azido-6-bromo-2-(4-(morpholine-4-carbonyl)phenyl)isonicotinate収率 275.9%

試薬・触媒・溶媒 1

HCID 6422
Trifluoroacetic acid
溶媒

実験手順

Methyl 3-amino-6-bromo-2-(4-(morpholine-4-carbonyl)phenyl)isonicotinate (2.00 gm, 4.76 mmol) was dissolved in trifluoroacetic acid (26 mL) and the yellow solution was cooled in an ice-bath. Powdered sodium nitrite (0.657 gm, 9.52 mmol) was added with stirring to give a dark red mixture. After 30 minutes, powdered sodium azide (3.09 gm, 47.6 mmol) was added followed by diethyl ether (26 mL). The light red mixture was stirred in the ice-bath for 30 minutes. The reaction was partitioned between EtOAc and sufficient saturated aqueous NaHCO3 solution (gas evolution) to neutralize the acid. The organic phase was washed with brine, dried over sodium sulfate, and concentrated to about 50 mL on the rotary evaporator. The resulting solid was collected by filtration and washed three times with EtOAc to give methyl 3-azido-6-bromo-2-(4-(morpholine-4-carbonyl)phenyl)isonicotinate (5.86 gm, 72% yield). Removal of the solvent from the filtrate followed by flash silica gel chromatography (step gradient elution with methylene chloride containing 0 to 2% MeOH) afforded another 1.58 gm of product. MS (ESI) m/z 446 and 448 (M+H). 1H NMR (CDCl3) δ ppm 7.82-7.80 (3H, m), 7.49-7.53 (2H, m), 4.02 (3H, s), 3.69-3.88 (4H, m), 3.57-3.70 (2H, m), 3.40-3.53 (2H, m).

後処理

  1. temperaturethe yellow solution was cooled in an ice-bath
  2. customto give a dark red mixture
  3. customThe reaction was partitioned between EtOAc and sufficient saturated aqueous NaHCO3 solution (gas evolution)
  4. washThe organic phase was washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated to about 50 mL on the rotary evaporator
  7. filtrationThe resulting solid was collected by filtration
  8. washwashed three times with EtOAc

出典と根拠

ORDレコード
ord-20b793b9645a41348e77894f21018f86
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815840B2

反応ノート

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