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3,5-Dibromopyridine → Tert-butyl 2-[(5-bromopyridin-3-yl)amino]-3-methylbutanoate

HRID 510176
ノート
印刷プレビュー

反応式

HRID 510176 の反応式
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Br:8])[CH:7]=1.Cl.[C:10]([O:14][C:15](=[O:21])[C@@H:16]([CH:18]([CH3:20])[CH3:19])[NH2:17])([CH3:13])([CH3:12])[CH3:11].CC(C)([O-])C.[Na+].C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Br:8][C:6]1[CH:7]=[C:2]([NH:17][CH:16]([CH:18]([CH3:20])[CH3:19])[C:15]([O:14][C:10]([CH3:12])([CH3:11])[CH3:13])=[O:21])[CH:3]=[N:4][CH:5]=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

7

反応物 4

HCID 693693,5-DibromopyridineHCID 634876Binap, (A+-)-HCID 23676156Sodium t-butoxideHCID 45108216H-D-Val-OtBu hydrochloride

生成物 1

HCID 89495408Tert-butyl 2-[(5-bromopyridin-3-yl)amino]-3-methylbutanoate収率 69.1%

試薬・触媒・溶媒 2

HCID 9811564
Bis(dibenzylideneacetone)palladium
触媒
HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

To a nitrogen degassed mixture of 3,5-dibromopyridine (5.0 g, 21.11 mmol), D-Valine t-butylester HCl (Aldrich Chemical, 4.43 g, 21.11 mmol) and sodium tert-butoxide (6.09 g, 63.3 mmol), in Toluene (200 ml) was added BINAP (2.63 g, 4.22 mmol) followed by tris(dibenzylideneacetone)-dipalladium(0) (Strem Chemical, 1.933 g, 2.111 mmol). The reaction was sealed and heated at 90° C. for 1 hr. The reaction was cooled, quenched into brine (100 mL), aqueous KHSO4 (20 mL) and ethyl acetate (200 mL). Aqueous sodium bicarbonate was added to adjust the pH to 8.0 and the organic layer removed. The aqueous layer was washed with ethyl acetate (100 mL). The combined organic extracts were washed with brine (100 mL), dried over sodium sulfate, filtered thru a pad of silica and the filtrate concentrated to oil. The oil was chromatographed on silica eluting with 5-30% ethyl acetate/hex to give 4.8 gm of compound I-2a, 69%.

後処理

  1. customTo a nitrogen degassed
  2. customThe reaction was sealed
  3. temperatureThe reaction was cooled
  4. customquenched into brine (100 mL), aqueous KHSO4 (20 mL) and ethyl acetate (200 mL)
  5. additionAqueous sodium bicarbonate was added
  6. customthe organic layer removed
  7. washThe aqueous layer was washed with ethyl acetate (100 mL)
  8. washThe combined organic extracts were washed with brine (100 mL)
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate concentrated to oil
  12. customThe oil was chromatographed on silica eluting with 5-30% ethyl acetate/hex

出典と根拠

ORDレコード
ord-8e57b07723a3472a81352d2a59121307
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09096598B2

反応ノート

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