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Boron Trichloride → HCID 178463348, 화합물

HRID 44116
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HRID 44116 반응식
C([O:8][C:9]1[C:14]([N:15]([CH2:20][CH3:21])[S:16]([CH3:19])(=[O:18])=[O:17])=[CH:13][N:12]2[N:22]=[C:23]([C:29]3[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=3)[C:24]([C:25]([NH:27][CH3:28])=[O:26])=[C:11]2[CH:10]=1)C1C=CC=CC=1.B(Cl)(Cl)Cl>ClCCl.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[CH2:20]([N:15]([C:14]1[C:9]([OH:8])=[CH:10][C:11]2[N:12]([N:22]=[C:23]([C:29]3[CH:30]=[CH:31][C:32]([F:35])=[CH:33][CH:34]=3)[C:24]=2[C:25]([NH:27][CH3:28])=[O:26])[CH:13]=1)[S:16]([CH3:19])(=[O:17])=[O:18])[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

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HCID 25135Boron TrichlorideHCID 67217877HCID 67217877, 화합물

생성물 1

HCID 178463348HCID 178463348, 화합물

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

5-(Benzyloxy)-6-(N-ethylmethylsulfonamido)-2-(4-fluorophenyl)-N-methylpyrazolo[1,5-a]pyridine-3-carboxamide (2.5 g, 5 mmol, 1 eq) was dissolved in dichloromethane and cooled to −78° C. Tetrabutylammonium iodide (0.19 g, 0.5 mmol, 0.1 eq) was added to the above mixture followed by slow dropwise addition of BCl3 (25 ml) at −78° C. The above solution was stirred at room temperature for 14 h. The solution was quenched with 10% sodium bicarbonate solution and the product was extracted with dichloromethane. The dichloromethane solution was evaporated to get off-brown solid. Yield: 1.6 g (79%). 1HNMR (400 MHz, DMSO-d6): δ 1.08 (t, J=7.14 Hz, 3H), 2.71 (d, J=4.52 Hz, 3H), 3.11 (s, 3H), 3.62 (q, J=6.92 Hz, 2H), 7.14 (s, 1H), 7.30 (t, J=8.86 Hz, 2H), 7.57 (d, J=4.56 Hz, 1H), 7.81-7.82 (m, 2H), 8.72 (s, 1H), 11.32 (br s, 1H). LCMS: (ES+) m/z=407.0 (M+H).

후처리

  1. customThe solution was quenched with 10% sodium bicarbonate solution
  2. extractionthe product was extracted with dichloromethane
  3. customThe dichloromethane solution was evaporated
  4. customto get off-brown solid

출처 및 근거

ORD 기록
ord-bf44313e25dd4758a80ffc094117f9cd
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536338B2

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