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Triphenylphosphine → N1-[4-(4-amino-1 tetrahydro-2H-4-pyranyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenyl]-2-fluoro-4-trifluoromethylbenzamide

HRID 897849
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HRID 897849 반응식
N(C(OCC)=O)=NC(OCC)=O.[NH2:13][C:14]1[N:19]=[CH:18][N:17]=[C:16]2[NH:20][N:21]=[C:22]([C:23]3[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:42])[C:31]4[CH:36]=[CH:35][C:34]([C:37]([F:40])([F:39])[F:38])=[CH:33][C:32]=4[F:41])=[C:25]([O:43][CH3:44])[CH:24]=3)[C:15]=12.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[O:64]1[CH2:69][CH2:68][CH:67](O)[CH2:66][CH2:65]1>O1CCCC1>[NH2:13][C:14]1[N:19]=[CH:18][N:17]=[C:16]2[N:20]([CH:67]3[CH2:68][CH2:69][O:64][CH2:65][CH2:66]3)[N:21]=[C:22]([C:23]3[CH:28]=[CH:27][C:26]([NH:29][C:30](=[O:42])[C:31]4[CH:36]=[CH:35][C:34]([C:37]([F:39])([F:40])[F:38])=[CH:33][C:32]=4[F:41])=[C:25]([O:43][CH3:44])[CH:24]=3)[C:15]=12
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참가 물질

6

반응물 4

HCID 11776Triphenylphosphine2회HCID 74956Tetrahydro-4H-pyran-4-ol2회HCID 220568ethyl N-ethoxycarbonyliminocarbamate2회HCID 178488248HCID 178488248, 화합물

생성물 1

HCID 20817390N1-[4-(4-amino-1 tetrahydro-2H-4-pyranyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenyl]-2-fluoro-4-trifluoromethylbenzamide수율 27.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Diethyl azodicarboxylate (0.07 mL, 0.45 mmol) was added into a mixture of N1-[4-(4-amino-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenyl]-2-fluoro-4-trifluoromethylbenzamide (0.10 g, 0.22 mmol), triphenylphosphine (0.12 g, 0.45 mmol) and tetrahydro-4H-pyran-4-ol (0.04 g, 0.34 mmol) in tetrahydrofuran (5 mL) and the mixture was stirred at ambient temperature overnight. Tetrahydro-4H-pyran-4-ol (0.01 g, 0.11 mmol), triphenylphosphine (0.04 g, 0.15 mmol) and diethyl azodicarboxylate (0.02 mL, 0.15 mmol) were added and the mixture was stirred at ambient temperature for 5 hours. The solvents were evaporated and the residue was purified by preparative HPLC to yield N1-[4-(4-amino-1-tetrahydro-2H-4-pyranyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-2-methoxyphenyl]-2-fluoro-4-trifluoromethylbenzamide (0.03 g, 0.06 mmol) as a white solid: 1H NMR (DMSO-d6 400 MHz) (9.91 (dd, 1H), 8.30(d, 1H), 8.25 (s, 1H), 8.00 (t, 1H), 7.89 (d, 1H), 7.75 (d, 1H), 7.34 (s, 1H), 7.31 (d, 1H), 6.90 (br, 2H), 4.95 (m, 1H), 4.02 (m, 2H), 3.95 (s, 3H), 3.56 (t, 2H), 2.22 (m, 2H), 1.89 (m, 2H);

후처리

  1. stirringthe mixture was stirred at ambient temperature for 5 hours
  2. customThe solvents were evaporated
  3. customthe residue was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-a847397345c247ca86e9a6ad527a99b8
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06921763B2

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