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Pyridine → Tert-butyl 2,6-dichloropyrimidine-4-carboxylate

HRID 1752395
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HRID 1752395 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8](Cl)=[O:9])[CH:5]=[C:4]([Cl:11])[N:3]=1.CCN(C(C)C)C(C)C.[C:21]([OH:25])([CH3:24])([CH3:23])[CH3:22].N1C=CC=CC=1>C(Cl)Cl>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([O:25][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:9])[CH:5]=[C:4]([Cl:11])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 6386tert-ButanolHCID 81531DiisopropylethylamineHCID 110311332,6-dichloropyrimidine-4-carbonyl Chloride

생성물 1

HCID 57285994Tert-butyl 2,6-dichloropyrimidine-4-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2,6-dichloropyrimidine-4-carbonyl chloride (1.026 g, 4.85 mmol) in DCM (25 mL) was added iPr2NEt (1.01 mL, 5.80 mmol) and t-butanol (0.51 mL, 5.3 mmol). The mixture was stirred overnight then pyridine (0.39 mL, 4.8 mmol) was added and the stirring continued over another night. The reaction mixture was evaporated in vacuo and the resulting residue was chromatographed over silica gel with 0-40% EtOAc in hexanes. The product fractions were evaporated in vacuo to give tert-butyl 2,6-dichloropyrimidine-4-carboxylate as a yellow-orange waxy solid (0.310 g, 1.24 mmol, 26% yield). 1H NMR (400 MHz, DMSO-d6): 8.15 (1H, s), 1.56 (9H, s). LC/MS: m/z=271.1 [M+Na]+.

후처리

  1. waitthe stirring continued over another night
  2. customThe reaction mixture was evaporated in vacuo
  3. customthe resulting residue was chromatographed over silica gel with 0-40% EtOAc in hexanes
  4. customThe product fractions were evaporated in vacuo

출처 및 근거

ORD 기록
ord-a135bad77da44fc996a1753a5d5a3b6e
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09163008B2

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