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Triisopropyl borate → tert-Butyl [5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)pyridin-2-yl]methylcarbamate

HRID 1851779
ノート
印刷プレビュー

反応式

HRID 1851779 の反応式
[Li]CCCC.Br[C:7]1[CH:8]=[CH:9][C:10]([CH2:13][NH:14][C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[N:11][CH:12]=1.C(O[B:26](OC(C)C)OC(C)C)(C)C.[OH:35][CH2:36][C:37]([CH3:41])([CH2:39][OH:40])[CH3:38]>C1COCC1>[CH3:38][C:37]1([CH3:41])[CH2:39][O:40][B:26]([C:7]2[CH:8]=[CH:9][C:10]([CH2:13][NH:14][C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[N:11][CH:12]=2)[O:35][CH2:36]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

6

反応物 4

HCID 21531Triisopropyl borateHCID 31344Neopentyl glycolHCID 45789881tert-Butyl ((5-bromopyridin-2-yl)methyl)carbamateHCID 178418339Butyllithium

生成物 1

HCID 86626541tert-Butyl [5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)pyridin-2-yl]methylcarbamate収率 11.3%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-78 °C

実験手順

n-BuLi (27 mL, 2.5 M) was slowly added to a stirred solution of tert-butyl (5-bromopyridin-2-yl)methylcarbamate (17.7 g, 61.6 mmol) in THF (280 mL) at −78° C. under an argon atmosphere. After 5 min at −78° C., triisopropylborate (28.5 mL, 123 mmol) was added and the mixture was stirred at −78° C. for 1 h. Neopentyl glycol (6.4 g, 61.4 mmol) was added and the reaction mixture was allowed to reach rt and was stirred for 2.5 d. The reaction was quenched with water (300 mL). The phases were separated and the aqueous phase was extracted with DCM. The organic layer was concentrated and the residue was purified by two successive flash chromatographies (Heptane/EtOAc 9:1→1:4 and DCM/MeOH 24:1 respectively) to give the product (2.23 g) as a white solid. 1H NMR 8.57 (dd, 1 H) 7.94 (dd, 1 H) 7.65 (dd, 1 H) 3.76 (s, 4 H) 3.30 (s, 3 H) 1.47 (s, 9 H) 0.96 (s, 6 H).

後処理

  1. customto reach rt
  2. stirringwas stirred for 2.5 d
  3. customThe reaction was quenched with water (300 mL)
  4. customThe phases were separated
  5. extractionthe aqueous phase was extracted with DCM
  6. concentrationThe organic layer was concentrated
  7. customthe residue was purified by two successive flash chromatographies (Heptane/EtOAc 9:1→1:4 and DCM/MeOH 24:1 respectively)

出典と根拠

ORDレコード
ord-37334a508a4f4ac491e95aa5e3251566
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08957215B2

反応ノート

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