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Sodium Carbonate → 3-chloro-N-[(R)-1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)propyl]-2-fluoro-benzamide

HRID 1517350
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HRID 1517350 반응식
[Cl:1][C:2]1[C:3]([F:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=O.[Cl-].ClC1N(C)C=C[N+]=1C.C(N(C(C)C)CC)(C)C.[Cl:30][C:31]1[CH:40]=[C:39]2[C:34]([C:35](=[O:67])[N:36]([NH:60][C:61]3[CH:66]=[CH:65][CH:64]=[CH:63][CH:62]=3)[C:37]([C@H:41]([NH:45][CH2:46][CH2:47][CH2:48][N:49]3[C:57](=[O:58])[C:56]4[C:51](=[CH:52][CH:53]=[CH:54][CH:55]=4)[C:50]3=[O:59])[CH2:42][C:43]#[CH:44])=[N:38]2)=[CH:33][CH:32]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C>[Cl:1][C:2]1[C:3]([F:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([N:45]([C@@H:41]([C:37]1[N:36]([NH:60][C:61]2[CH:66]=[CH:65][CH:64]=[CH:63][CH:62]=2)[C:35](=[O:67])[C:34]2[C:39](=[CH:40][C:31]([Cl:30])=[CH:32][CH:33]=2)[N:38]=1)[CH2:42][C:43]#[CH:44])[CH2:46][CH2:47][CH2:48][N:49]1[C:50](=[O:59])[C:51]2[C:56](=[CH:55][CH:54]=[CH:53][CH:52]=2)[C:57]1=[O:58])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 10340Sodium CarbonateHCID 81531Diisopropylethylamine2회HCID 3029313-Chloro-2-fluorobenzoic acidHCID 111266512-chloro-1,3-dimethyl-1H-imidazol-3-ium chlorideHCID 57695432(R)-2-{3-[1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynylamino]-propyl}-isoindole-1,3-dione

생성물 1

HCID 57695459
3-chloro-N-[(R)-1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)propyl]-2-fluoro-benzamide
수율 96%

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

To a solution of 3-chloro-2-fluoro-benzoic acid (3.2 g, 18.3 mmol) of in acetonitrile (30 ml) was added 2-chloro-1,3-dimethylimidazolium chloride (DMC) (3.3 g, 19.5 mmol), followed by diisopropylethyl amine (6.8 ml, 39 mmol). The resulted solution was stirred at room temperature for 10 min, then transferred into flask containing (R)-2-{3-[1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynylamino]-propyl}-isoindole-1,3-dione (6.1 g) in a 2.5M solution of diisopropylethyl amine in acetonitrile (30 ml). The reaction mixture was stirred at room temperature and the reaction progress was monitored by HPLC/MS. Upon completion, a saturated solution of sodium carbonate (100 ml) was added. The organic layers were collected and the aqueous layer was washed with EtOAc (2×50 ml). The combined organic layers were washed with brine (100 ml) and dried over sodium sulfate. The solvent was removed and residue was separated on silica gel column to afford 3-chloro-N-[(R)-1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)propyl]-2-fluoro-benzamide as off-white solid (7.6 g, 96%). M.p. 130-132° C. LCMS: m/e 682 [M+H]. 1H NMR (CDCl3): δ 8.09 (m, 1H), 7.71 (m, 3H), 7.46 (m, 1H), 7.35 (m, 2H), 7.29 (m, 1H), 7.16 (m, 1H), 7.10 (m, 1H), 7.03 (m, 1H), 6.90 (m, 1H), 6.82 (m, 1H), 6.68 (m, 1H), 6.50 (m, 1H), 3.73 (m, 1H), 3.58 (m, 1H), 3.51 (m, 1H), 3.38 (m, 1H), 3.26 (m, 1H), 3.06 (m, 1H), 2.88 (m, 1H), 2.01 (s, 1H), 1.80 (m, 1H), 1.54 (m, 1H).

후처리

  1. customtransferred into flask
  2. stirringThe reaction mixture was stirred at room temperature
  3. customThe organic layers were collected
  4. washthe aqueous layer was washed with EtOAc (2×50 ml)
  5. washThe combined organic layers were washed with brine (100 ml)
  6. dry with materialdried over sodium sulfate
  7. customThe solvent was removed
  8. customresidue was separated on silica gel column

출처 및 근거

ORD 기록
ord-9f67d1fcb3fb4bec92c0e84130366c1c
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232285B2

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