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Phosphorus oxychloride → Hydrochloric Acid

HRID 1970993
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HRID 1970993 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6]3[C:14](=O)[NH:13][CH:12]=[C:11]([C:16]#[N:17])[C:7]=3[NH:8][C:9]=2[CH:10]=1.O=P(Cl)(Cl)[Cl:20]>O1CCOCC1>[Cl:20][C:14]1[C:6]2[C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:10][C:9]=3[NH:8][C:7]=2[C:11]([C:16]#[N:17])=[CH:12][N:13]=1.[ClH:1]
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참가 물질

5

반응물 2

HCID 24813Phosphorus oxychlorideHCID 565951917-chloro-1-oxo-2,5-dihydro-1H-pyrido[4,3-b]indole-4-carbonitrile

생성물 2

HCID 313Hydrochloric AcidHCID 565950571,7-dichloro-5H-pyrido[4,3-b]indole-4-carbonitrile

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
93 °C

실험 절차

To a slurry of 7-chloro-1-oxo-2,5-dihydro-1H-pyrido[4,3-b]indole-4-carbonitrile (24.95 g, 102 mmol) in dioxane (200 mL) was added POCl3 (79 g, 512 mmol) dropwise at 93° C. The reaction mixture was left to stir at 93° C. for 5 h, cooled to room temperature, and left to stir overnight. The reaction mixture was filtered, washed with MTBE, and dried to give the title compound as an HCl salt. 1H NMR (600 MHz, CD3SOCD3) δ 13.33 (s, 1H); 8.80 (s, 1H); 8.39 (d, 1H); 7.70 (d, 1H); 7.50 (dd, 1H). LRMS (APCI) calc'd for (C12H5Cl2N3) [M+H]+, 262.0. found 261.9.

후처리

  1. waitThe reaction mixture was left
  2. temperaturecooled to room temperature
  3. waitleft
  4. stirringto stir overnight
  5. filtrationThe reaction mixture was filtered
  6. washwashed with MTBE
  7. customdried

출처 및 근거

ORD 기록
ord-db93b9f5d6fb41339b92e8d508a93500
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431569B2

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