Sodium Chloride → 2-ethoxy-5-(3-(1-hydroxy-2,3-dihydro-1H-inden-4-yl)-1,2,4-oxadiazol-5-yl)benzonitrile

HRID 1048934노트

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HRID 1048934 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH2:13][CH3:14])[C:6]([OH:8])=O)#[N:2].C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.O[N:37]=[C:38]([C:40]1[C:41]2[CH2:42][CH2:43][CH:44]([OH:49])[C:45]=2[CH:46]=[CH:47][CH:48]=1)[NH2:39].[Na+].[Cl-]>CN(C=O)C>[CH2:13]([O:12][C:11]1[CH:10]=[CH:9][C:5]([C:6]2[O:8][N:39]=[C:38]([C:40]3[CH:48]=[CH:47][CH:46]=[C:45]4[C:41]=3[CH2:42][CH2:43][CH:44]4[OH:49])[N:37]=2)=[CH:4][C:3]=1[C:1]#[N:2])[CH3:14]

참가 물질

7

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온도
130 °C

실험 절차

In a microwave vial, a stirring solution of 3-cyano-4-ethoxybenzoic acid (200 mg, 1.05 mmol) in DMF was treated with HOBt (185 mg, 1.36 mmol) and EDCI (260 mg, 1.36 mmol) at room temperature. The reaction was stirred for 20 min followed by addition, in a single portion, of N′,1-dihydroxy-2,3-dihydro-1H-indene-4-carboximidamide (261 mg, 1.36 mmol). The reaction was stirred for additional 30 min at room temperature and then heated to 130° C. for 35 min in the initiator. The reaction was diluted using a saturated solution of NaCl and extracted with EtOAc (80 ml×3). The organic phase was dried over Na2SO4 anhydrous and concentrated under reduced pressure. The product was purified by column chromatography using CH2Cl2:MeOH (9:1) to offer the product as pale yellow solid in 79% yield (274 mg).

후처리

  1. stirringThe reaction was stirred for additional 30 min at room temperature
  2. additionThe reaction was diluted
  3. extractionextracted with EtOAc (80 ml×3)
  4. dry with materialThe organic phase was dried over Na2SO4 anhydrous
  5. concentrationconcentrated under reduced pressure
  6. customThe product was purified by column chromatography

출처 및 근거

ORD 기록
ord-27e358e5c67a4c51b20a6729d4c077c9
출처 데이터셋
uspto-grants-2016_07
특허 번호
US09382217B2

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