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Sodium Bicarbonate → 4-Chloro-6-methoxy-7-(2-piperidinoethoxy)quinazoline

HRID 1791701
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인쇄 미리보기

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HRID 1791701 반응식
Cl.[Cl:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH2:16][CH2:17][N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[CH:5][N:4]=1.C(=O)([O-])O.[Na+]>C(Cl)Cl>[Cl:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH2:16][CH2:17][N:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[C:10]([O:13][CH3:14])[CH:11]=2)[N:6]=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 220308104-Chloro-6-methoxy-7-(2-piperidinoethoxy)quinazoline hydrochloride

생성물 1

HCID 110885414-Chloro-6-methoxy-7-(2-piperidinoethoxy)quinazoline

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-Chloro-6-methoxy-7-(2-piperidinoethoxy)quinazoline hydrochloride was suspended in methylene chloride (10 ml) and saturated aqueous sodium hydrogen carbonate solution (5 ml) then stirred vigorously for 10 minutes at ambient temperature. The layers were separated and the organic layer dried (MgSO4) then evaporated to give a white solid. This solid was triturated with methanol (2.5 ml), the resulting solid filtered off, washed with cold methanol and dried to give 4-chloro-6-methoxy-7-(2-piperidinoethoxy)quinazoline (0.36 g).

후처리

  1. customThe layers were separated
  2. dry with materialthe organic layer dried (MgSO4)
  3. customthen evaporated
  4. customto give a white solid
  5. customThis solid was triturated with methanol (2.5 ml)
  6. filtrationthe resulting solid filtered off
  7. washwashed with cold methanol
  8. customdried

출처 및 근거

ORD 기록
ord-8e3da567cf4548409d45d737a189f0dc
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074800B1

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