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Sodium Azide → Azido-PEG6-C1-Boc

HRID 1726833
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HRID 1726833 반응식
[N-:1]=[N+:2]=[N-:3].[Na+].[C:5]([O:9][C:10](=[O:31])[CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29]Br)([CH3:8])([CH3:7])[CH3:6]>CN(C=O)C>[C:5]([O:9][C:10](=[O:31])[CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][N:1]=[N+:2]=[N-:3])([CH3:8])([CH3:7])[CH3:6]
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참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 86616366Br-PEG6-CH2COOtBu

생성물 1

HCID 10905931Azido-PEG6-C1-Boc수율 57.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

Sodium azide (1.5 g, 23 mmol) was added to a solution of compound 3 (1.9 g, 4.1 mmol) in dry DMF (50 mL) and the resulting mixture was stirred at 80° C. overnight. The reaction mixture was concentrated in vacuo and then triturated with CH2Cl2 (20 mL) and filtered to remove sodium azide. The filtrate was concentrated in vacuo and the residue was loaded onto a silica gel gravity column (200 g) and eluted with CH2Cl2:MeOH 100:0 to 20:1 (v/v) to afford compound 4 as a colorless oil (1.0 g, 57%).

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customtriturated with CH2Cl2 (20 mL)
  3. filtrationfiltered
  4. customto remove sodium azide
  5. concentrationThe filtrate was concentrated in vacuo
  6. washeluted with CH2Cl2:MeOH 100:0 to 20:1 (v/v)

출처 및 근거

ORD 기록
ord-4bcfd1eec923431f919e1cbd0bf9dcb2
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07494714B2

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