ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Cesium carbonate → [5-((R)-3-hydroxy-pyrrolidin-1-ylmethyl)-pyridin-2-yl]carbamic acid tert-butyl ester

HRID 43133
ノート
印刷プレビュー

反応式

HRID 43133 の反応式
[OH:1][C@@H:2]1[CH2:6][CH2:5][NH:4][CH2:3]1.[C:7]([O:11][C:12](=[O:22])[NH:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20]Br)=[CH:16][N:15]=1)([CH3:10])([CH3:9])[CH3:8].C([O-])([O-])=O.[Cs+].[Cs+]>CN(C=O)C>[C:7]([O:11][C:12](=[O:22])[NH:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][N:4]2[CH2:5][CH2:6][C@@H:2]([OH:1])[CH2:3]2)=[CH:16][N:15]=1)([CH3:10])([CH3:9])[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10796Cesium carbonateHCID 2759337(R)-3-PyrrolidinolHCID 23030321tert-Butyl (5-(bromomethyl)pyridin-2-yl)carbamate

生成物 1

HCID 66914597[5-((R)-3-hydroxy-pyrrolidin-1-ylmethyl)-pyridin-2-yl]carbamic acid tert-butyl ester収率 41.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of (5-methyl-pyridin-2-yl)-carbamic acid tert-butyl ester (Step 100.3) (10.7 g, 51.4 mmol), NBS (10.1 g, 56.7 mmol, 1.1 equiv), AIBN (843 mg, 5.14 mmol, 0.1 equiv) in CCl4 (500 mL) was stirred for 1 h at relfux. NBS (1.8 g, 10.1 mmol, 0.2 equiv) was added and the mixture was stirred at reflux for additional 30 min. The reaction mixture was filtered hot and the filtrate was concentrated. Trituration of the residue in CH3CN afforded of 12.88 g of impure (5-bromomethyl-pyridin-2-yl)-carbamic acid tert-butyl ester (intermediate 100.2). (R)-3-Hydroxypyrrolidine (181 mg, 2.1 mmol, 1.2 equiv) was added to a mixture of intermediate 100.2 (500 mg, 1.75 mmol) and Cs2CO3 (684 mg, 2.1 mmol, 1.2 equiv) in DMF (5 ml). The reaction mixture was stirred for 24 h at rt, quenched by addition of a saturated aqueous solution of NaHCO3 (150 mL) and extracted with EtOAc. The organic layer was washed with a saturated aqueous solution of NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (DCM/NH3aq, 99:1→DCM/MeOH/NH3aq, 96:3:1) to afford 212 mg of the title compound as a white solid. Title compound: ESI-MS: 294.3 [M+H]+; tR=1.95 min (System 1); TLC: Rf=0.14 (DCM/MeOH, 9:1).

後処理

  1. customquenched by addition of a saturated aqueous solution of NaHCO3 (150 mL)
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed with a saturated aqueous solution of NaHCO3
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography (DCM/NH3aq, 99:1→DCM/MeOH/NH3aq, 96:3:1)

出典と根拠

ORDレコード
ord-f2a83dbf186840b1b4dc2e68895fb5ed
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08536175B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート