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Ethyl bromopyruvate → Ethyl 6-chloro-5-[(diethoxyphosphinyl)methyl]imidazo[1,2-a]pyridine-2-carboxylate

HRID 861992
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반응식

HRID 861992 반응식
[NH2:1][C:2]1[N:7]=[C:6]([CH2:8][P:9](=[O:16])([O:13][CH2:14][CH3:15])[O:10][CH2:11][CH3:12])[C:5]([Cl:17])=[CH:4][CH:3]=1.Br[CH2:19][C:20](=O)[C:21]([O:23][CH2:24][CH3:25])=[O:22]>COCCOC.CCO>[Cl:17][C:5]1[CH:4]=[CH:3][C:2]2[N:7]([CH:19]=[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[N:1]=2)[C:6]=1[CH2:8][P:9]([O:13][CH2:14][CH3:15])([O:10][CH2:11][CH3:12])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 66144Ethyl bromopyruvateHCID 86752043Diethyl [(6-amino-3-chloro-2-pyridinyl)methyl]phosphonate

생성물 1

HCID 19701397Ethyl 6-chloro-5-[(diethoxyphosphinyl)methyl]imidazo[1,2-a]pyridine-2-carboxylate수율 13%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 80711,2-Dimethoxyethane용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

Following the procedure for Example 17, the residue from Example 28 was combined with ethyl bromopyruvate (0.468 g, 2.4 mmol) in DME (25 mL). After the resulting salt was refluxed in abs EtOH (30 mL) for 6 h, workup and puricication produced 0./114 g (13% of title compound).

후처리

  1. customworkup and puricication produced 0

출처 및 근거

ORD 기록
ord-277790dcd3c24a0ba46626ad1f117d97
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05716964

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