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tert-Butanol → Ammonium Hydroxide

HRID 1615806
ノート
印刷プレビュー

反応式

HRID 1615806 の反応式
[O:1]=[C:2]1[NH:10][C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]21[CH2:21][C:13]1[CH:14]=[N:15][C:16](C([O-])=O)=[CH:17][C:12]=1[CH2:11]2.[Na+].C([N:25]([CH2:28]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:37])C=CC=CC=1.[C:47]([OH:51])([CH3:50])([CH3:49])[CH3:48]>>[NH4+:6].[OH-:1].[O:1]=[C:2]1[NH:10][C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]21[CH2:21][C:13]1[CH:14]=[N:15][C:16]([NH:25][C:28](=[O:37])[O:51][C:47]([CH3:50])([CH3:49])[CH3:48])=[CH:17][C:12]=1[CH2:11]2
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 6386tert-ButanolHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azide2 回HCID 57974026(+/-)-Sodium 2'-oxo-1',2',5,7-tetrahydrospiro[cyclopenta[c]pyridine-6,3'-pyrrolo[2,3-b]pyridine]-3-carboxylate2 回

生成物 2

HCID 14923Ammonium Hydroxide
HCID 86616403
(+/-)-Tert-butyl(2'-oxo-1',2',5,7-tetrahydrospiro[cyclopenta[c]pyridine-6,3'-pyrrolo[2,3-b]pyridin]-3-yl)carbamate

実験手順

To a suspension of (±)-sodium 2′-oxo-1′,2′,5,7-tetrahydrospiro[cyclopenta[c]pyridine-6,3′-pyrrolo[2,3-b]pyridine]-3-carboxylate (1.64 g, 5.83 mmol, described in Intermediate 7) and triethylamine (1.62 mL, 11.7 mmol) in tert-butanol (50 mL) was added diphenylphosphoryl azide (1.89 mL, 8.75 mmol) and the mixture was heated at reflux for 72 h. Additional diphenylphosphoryl azide (1.89 mL, 8.75 mmol) was added after 24 h and 56 h. The reaction mixture was concentrated in vacuo and then partitioned between CH2Cl2 (75 mL) and saturated NaHCO3 (100 mL). The organic layer was separated and the aqueous layer was further extracted with CH2Cl2 (2×50 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH: NH4OH—100:0:0 to 95:5:1, to give the title compound. MS: m/z=353 (M+1).

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 72 h
  3. concentrationThe reaction mixture was concentrated in vacuo
  4. custompartitioned between CH2Cl2 (75 mL) and saturated NaHCO3 (100 mL)
  5. customThe organic layer was separated
  6. extractionthe aqueous layer was further extracted with CH2Cl2 (2×50 mL)
  7. dry with materialThe combined organic layers were dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe crude product was purified by silica gel chromatography
  11. washeluting with a gradient of CH2Cl2

出典と根拠

ORDレコード
ord-3be143d9a1c34366b12b322e9d70768b
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765759B2

反応ノート

読み込み中…

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