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Dimethylformamide → HCID 58746070, 화합물

HRID 2378471
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HRID 2378471 반응식
[C:1]([O:5][C:6](=[O:18])[NH:7][C:8]1[C:9]2[N:10]([N:15]=[CH:16][CH:17]=2)[C:11](I)=[CH:12][CH:13]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:19][N:20](C=O)C>[C-]#N.[Zn+2].[C-]#N.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:1]([O:5][C:6](=[O:18])[NH:7][C:8]1[C:9]2[N:10]([N:15]=[CH:16][CH:17]=2)[C:11]([C:19]#[N:20])=[CH:12][CH:13]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

5

반응물 2

HCID 6228DimethylformamideHCID 58746000HCID 58746000, 화합물

생성물 1

HCID 58746070HCID 58746070, 화합물수율 93%

시약·촉매·용매 2

HCID 11186Zinc cyanide (Zn(CN)2)촉매HCID 11979704Tetrakis(triphenylphosphine)palladium촉매

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온도
80 °C

실험 절차

A mixture of (7-iodo-pyrazolo[1,5-a]pyridin-4-yl)-carbamic acid tert-butyl ester (36 mg, 0.1 mmol), zinc cyanide (24 mg, 0.2 mmol), tetrakis(triphenylphosphine) palladium (0) (23 mg, 0.02 mmol), and anhydrous DMF (1 mL) was degassed with argon. Then, the mixture was stirred at 80° C. for 4.5 h, cooled to rt, mixed with EtOAc (6 mL), and filtered. The filtrate was concentrated under reduced pressure. Purification by silica gel flash chromatography eluting with EtOAc/heptane (gradient from 1:4 to 1:2 ratio) gave compound 777E (24 mg, 93%) as a white solid. HPLC: 93% at 3.64 min (retention time) (YMC S5 ODS-A column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 mincontaining 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 259 [M+H]+.

후처리

  1. customwas degassed with argon
  2. temperaturecooled to rt
  3. additionmixed with EtOAc (6 mL)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customPurification by silica gel flash chromatography
  7. washeluting with EtOAc/heptane (gradient from 1:4 to 1:2 ratio)

출처 및 근거

ORD 기록
ord-28931f286fed4060af5b3f613b5a1472
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07470797B2

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