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O-Toluidine → HCID 10332347, 화합물

HRID 973564
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HRID 973564 반응식
[NH2:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[NH2:13][C:14]1[C:15]([CH3:20])=[CH:16][CH:17]=[CH:18][CH:19]=1>C(O)C>[NH2:1][C:2]1[N:11]=[C:10]([NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[CH3:20])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7242O-ToluidineHCID 104422884-Chloroquinazolin-2-amine

생성물 1

HCID 10332347HCID 10332347, 화합물수율 62%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Amino-4-chloroquinazoline (0.64 g, 0.0036 mol) was heated to 170° in o-toluidine (1 ml, 0.008 mol) for 1 hour. The reaction mixture was dissolved in ethanol, stripped and partitioned between chloroform and NaOH solution (pH 9). The organic solution was dried, filtered and excess solvent removed to give an oil which afforded crystals of 2-amino-4-(2-methylphenylamino)-quinazoline (0.55 g, 62%) m.p. 273°-275° (from ethanol).

후처리

  1. custompartitioned between chloroform and NaOH solution (pH 9)
  2. customThe organic solution was dried
  3. filtrationfiltered
  4. customexcess solvent removed
  5. customto give an oil which

출처 및 근거

ORD 기록
ord-fe260666ec40421e802a18037708db9a
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05064833

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