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Oxalyl chloride → 6-Chloro-2-fluoro-3-(pivalamidomethyl)benzoyl isocyanate

HRID 508834
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인쇄 미리보기

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HRID 508834 반응식
[Cl:1][C:2]1[C:7]([C:8]([NH2:10])=[O:9])=[C:6]([F:11])[C:5]([CH2:12][NH:13][C:14](=[O:19])[C:15]([CH3:18])([CH3:17])[CH3:16])=[CH:4][CH:3]=1.C(Cl)(=O)[C:21](Cl)=[O:22]>C(Cl)CCl>[Cl:1][C:2]1[C:7]([C:8]([N:10]=[C:21]=[O:22])=[O:9])=[C:6]([F:11])[C:5]([CH2:12][NH:13][C:14](=[O:19])[C:15]([CH3:16])([CH3:18])[CH3:17])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 900195026-Chloro-2-fluoro-3-(pivalamidomethyl)benzamide

생성물 1

HCID 900197456-Chloro-2-fluoro-3-(pivalamidomethyl)benzoyl isocyanate수율 307.5%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

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온도
65 °C

실험 절차

To a solution of 6-chloro-2-fluoro-3-(pivalamidomethyl)benzamide (0.300 g, 1.04 mmol) in EDC (10 mL) was added oxalyl chloride (0.11 mL, 1.25 mmol). The reaction mass was heated at 60-70° C. for 4-5 h. Excess of solvent was removed under vacuum to afford 1.0 g of desired product.

후처리

  1. customExcess of solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-2da01bbf67b94645a6b7413da201026c
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096545B2

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