Triethylamine → (5,7-Dibromo-adamantan-2-yl)-carbamic acid tert-butyl ester

HRID 1505294ノート

反応式

HRID 1505294 の反応式
[Br:1][C:2]12[CH2:12][CH:6]3[CH2:7][C:8]([Br:11])([CH2:10][CH:4]([CH:5]3C(O)=O)[CH2:3]1)[CH2:9]2.CCN(CC)CC.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[CH3:40][C:41]([O-:44])([CH3:43])[CH3:42].[K+].[N-:46]=[C:47]=[O:48]>C1(C)C=CC=CC=1.C1COCC1>[C:41]([O:44][C:47](=[O:48])[NH:46][CH:5]1[CH:4]2[CH2:10][C:8]3([Br:11])[CH2:9][C:2]([Br:1])([CH2:12][CH:6]1[CH2:7]3)[CH2:3]2)([CH3:43])([CH3:42])[CH3:40]

参加物

8

反応物 5

HCID 8471TriethylamineHCID 105034IsocyanateHCID 199401P,P-Diphenylphosphinic azideHCID 149770365,7-Dibromoadamantane-2-carboxylic acidHCID 23665647Potassium tert-butoxide

生成物 1

HCID 16100375(5,7-Dibromo-adamantan-2-yl)-carbamic acid tert-butyl ester

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
85 °C

実験手順

A suspension of the acid 24 (2.00 g, 5.92 mmol) in dry toluene (30 mL) was treated successively with Et3N (1.0 mL, 7.10 mmol) and diphenylphosphoryl azide (DPPA, 1.6 mL, 7.10 mmol). The resulting mixture was stirred at 85° C. for 15 h. To a separated flask containing a solution of t-BuOK (1.35 g, 11.8 mmol) in dry THF (80 mL) at 0° C. was added the isocyanate solution dropwise via a dropping funnel. The resulting reaction mixture was allowed to warm to rt over 30 min, and then it was quenched with water. The THF was removed in vacuo, and the resulting material was diluted with EtOAc. The organic layer was washed with 1N HCl, sat. NaHCO3 and brine, dried (Na2SO4), filtered and concentrated in vacuo. Flash chromatography (SiO2, 95:5 to 8:2, hexanes/EtOAc) afforded 1.20 g (50%, 2 steps) of the title compound as a white powder. 1H NMR (300 MHz, CDCl3) δ 4.68 (bs, 1 H), 3.76 (bs, 1 H), 2.87 (s, 2 H), 2.47-2.13 (m, 10 H), 1.46 (s, 9 H).

後処理

  1. customThe resulting reaction mixture
  2. temperatureto warm to rt over 30 min
  3. customit was quenched with water
  4. customThe THF was removed in vacuo
  5. additionthe resulting material was diluted with EtOAc
  6. washThe organic layer was washed with 1N HCl, sat. NaHCO3 and brine
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-c5254ccb20f1456796bf3dbf84dfa7f0
出典データセット
uspto-grants-2015_12
特許番号
US09216976B2

反応ノート

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