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Thiourea → HCID 66820877, 화합물

HRID 2196463
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HRID 2196463 반응식
[Cl:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]#[N:11])=[CH:5][CH:4]=1.[NH2:12][C:13]([NH2:15])=[S:14]>CO>[ClH:1].[C:10]([CH2:9][C:6]1[CH:7]=[CH:8][C:3]([CH2:2][S:14][C:13](=[NH:12])[NH2:15])=[CH:4][CH:5]=1)#[N:11]
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참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 117449912-(4-(Chloromethyl)phenyl)acetonitrile

생성물 1

HCID 66820877HCID 66820877, 화합물수율 75.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The 4-chloromethylphenylacetonitrile (200 mg, 1.21 mmol) and thiourea (101 mg, 1.33 mmol) were mixed in 1 ml of methanol. The mixture was heated to reflux for 3 to 4 hours. The reaction mixture was evaporated. After that, 1 ml of methanol and 4 ml of acetone were added and the mixture was stirred for one hour. The crystalline material was filtered and the product was dried under high vacuum overnight to yield 219 mg (0.91 mmol, yield 75%) of product as off white crystals, with purity greater than 95%. 1H NMR (300 MHz, d6-DMSO) 4.03 (s, 2H), 4.50 (s, 2H), 7.35 (d, 2H, J=8.23 Hz), 7.45 (d, 2H, J=8.23 Hz), 9.22 (s, 4H). (M+H) 206.00

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 3 to 4 hours
  3. customThe reaction mixture was evaporated
  4. additionAfter that, 1 ml of methanol and 4 ml of acetone were added
  5. filtrationThe crystalline material was filtered
  6. customthe product was dried under high vacuum overnight

출처 및 근거

ORD 기록
ord-77e6d2db69d0471f8e732c0722c1a9a3
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338454B2

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