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Diethyl Ether → Methyl 3-azido-6-bromo-6'-morpholino-2,3'-bipyridine-4-carboxylate

HRID 2410752
ノート
印刷プレビュー

反応式

HRID 2410752 の反応式
[NH2:1][C:2]1[C:3]([C:13]2[CH:14]=[N:15][C:16]([N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)=[CH:17][CH:18]=2)=[N:4][C:5]([Br:12])=[CH:6][C:7]=1[C:8]([O:10][CH3:11])=[O:9].N([O-])=O.[Na+].[N-:29]=[N+:30]=[N-].[Na+].CCOCC>C(O)(C(F)(F)F)=O.O>[N:1]([C:2]1[C:3]([C:13]2[CH:14]=[N:15][C:16]([N:19]3[CH2:20][CH2:21][O:22][CH2:23][CH2:24]3)=[CH:17][CH:18]=2)=[N:4][C:5]([Br:12])=[CH:6][C:7]=1[C:8]([O:10][CH3:11])=[O:9])=[N+:29]=[N-:30]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 3283Diethyl EtherHCID 33557Sodium AzideHCID 23668193Sodium NitriteHCID 86663022Methyl 3-amino-6-bromo-6'-morpholino-2,3'-bipyridine-4-carboxylate

生成物 1

HCID 86663023Methyl 3-azido-6-bromo-6'-morpholino-2,3'-bipyridine-4-carboxylate収率 98%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6422Trifluoroacetic acid溶媒

実験手順

Methyl 3-amino-6-bromo-6′-morpholino-2,3′-bipyridine-4-carboxylate (230 mg, 0.59 mmol) was dissolved in TFA (2.9 mL) and the solution was cooled in an ice bath. Solid sodium nitrite (89 mg, 1.29 mmol) was added slowly with stirring to give a red solution. After 30 min, powdered sodium azide (380 mg, 5.85 mmol) was added in portions with gas evolution. Et2O (29 mL) was added with stirring after 0.5 hr, water was added and the mixture was extracted with EtOAc. The combined organic extracts were washed with, water (3×), saturated Na2CO3 solution (until the aqueous phase was basic), and brine (1×). After drying the solvent with sodium sulfate, the solvent was removed. Flash chromatography (step gradient elution with DCM containing 0 to 20% EtOAc) afforded methyl 3-azido-6-bromo-6′-morpholino-2,3′-bipyridine-4-carboxylate (240 mg, 0.57 mmol, 98% yield) yellow solid. 1H NMR (500 MHz, chloroform-d) δ ppm 8.73 (1H, d, J=2.44 Hz), 7.99 (1H, dd, J=9.00, 2.59 Hz), 7.71 (1H, s), 6.68 (1H, d, J=8.85 Hz), 4.00 (3H, s), 3.79-3.86 (4H, m), 3.59-3.66 (4H, m).

後処理

  1. temperaturethe solution was cooled in an ice bath
  2. customto give a red solution
  3. stirringwith stirring after 0.5 hr
  4. extractionthe mixture was extracted with EtOAc
  5. washThe combined organic extracts were washed with, water (3×), saturated Na2CO3 solution (until the aqueous phase
  6. dry with materialAfter drying the solvent with sodium sulfate
  7. customthe solvent was removed
  8. washFlash chromatography (step gradient elution with DCM containing 0 to 20% EtOAc)

出典と根拠

ORDレコード
ord-66317d6883524e70b31e53e571173fac
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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