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Benzoyl chloride → 2,5-Bis(4-benzamidophenyl)furan

HRID 1295203
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HRID 1295203 반응식
Cl.Cl.C(NC1C=CC(C2[O:19][C:20]([C:23]3[CH:28]=[CH:27][C:26](NC(=N)C4C=CC=CC=4)=[CH:25][CH:24]=3)=CC=2)=CC=1)(=N)C1C=CC=CC=1.[NH2:38][C:39]1[CH:44]=[CH:43][C:42]([C:45]2[O:46][C:47]([C:50]3[CH:55]=[CH:54][C:53]([NH2:56])=[CH:52][CH:51]=3)=[CH:48][CH:49]=2)=[CH:41][CH:40]=1.C(N(CC)CC)C.[C:64](Cl)(=[O:71])[C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1>C(#N)C.O>[C:64]([NH:56][C:53]1[CH:54]=[CH:55][C:50]([C:47]2[O:46][C:45]([C:42]3[CH:43]=[CH:44][C:39]([NH:38][C:20](=[O:19])[C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=4)=[CH:40][CH:41]=3)=[CH:49][CH:48]=2)=[CH:51][CH:52]=1)(=[O:71])[C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 7412Benzoyl chlorideHCID 8471TriethylamineHCID 120498462,5-Bis(4-aminophenyl)furanHCID 178478770HCID 178478770, 화합물2회

생성물 1

HCID 105826602,5-Bis(4-benzamidophenyl)furan수율 96%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6342Acetonitrile용매

실험 절차

2,5-Bis[4-(benzimidoylamino)phenyl]furan Dihydrochloride (Compound 6b) To a chilled solution of 2,5-bis(4-aminophenyl)furan (0.25 g, 1.0 mmol) in dry acetonitrile (10 ml) was added triethylamine (0.22 g, 2.1 mmol) followed dropwise by benzoyl chloride (0.30 g, 2.1 mmol) and the resulting suspension was stirred at room-temperature for 3 hours. Water (10 ml) was then added and the precipitate was collected, rinsed with water, followed by MeOH, and finally dried in vacuo to give 2,5-bis(4-benzamidophenyl)furan as a tan solid (0.44 g, 96%), mp 312-314.5° C. 1H NMR (DMSO-d6): 6.98 (s, 2H), 7.52-7.62 (m, 6H), 7.80 (d, 4H), 7.89 (d, 4H), 7.97 (d, 4H), 10.33 (br s, 2H).

후처리

  1. customthe precipitate was collected
  2. washrinsed with water
  3. customfinally dried in vacuo

출처 및 근거

ORD 기록
ord-c01c5f5b91df478e8ec84cce3aa26b22
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241795B2

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