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Ammonia → 5-Quinazolinol, 2-methyl- (9CI)

HRID 495435
ノート
印刷プレビュー

反応式

HRID 495435 の反応式
C[O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[N:6][C:7]([CH3:13])=[N:8]2.B(Br)(Br)Br.N>ClCCl>[OH:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[N:6][C:7]([CH3:13])=[N:8]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 222AmmoniaHCID 25134Boron tribromideHCID 22326675HCID 22326675、化合物

生成物 1

HCID 1355530175-Quinazolinol, 2-methyl- (9CI)収率 15%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
20 °C

実験手順

To a stirred solution of 5-methoxy-2-methylquinazoline (0.22 g, 1.26 mmol) in dichloromethane (20 mL) at 0° C. under argon was added a solution of boron tribromide in dichloromethane (1M, 3.8 mL), dropwise over 0.01 h. The resulting mixture was stirred at 20° C. for 48 h then poured into a mixture of ice (50 g) and 0.880 aqueous ammonia (50 mL) and stirred for 0.5 h. Organic phase was separated and aqueous phase washed with dichloromethane (3×30 mL). The aqueous phase was acidified (pH 6) with citric acid and the resulting mixture extracted with ethyl acetate (3×50 mL). The combined ethyl acetate extracts were dried (Na2SO4) and evaporated in vacuo to give the title compound (0.030 g, 15%) as an oil which was used without further purification.

後処理

  1. stirringstirred for 0.5 h
  2. customOrganic phase was separated
  3. washaqueous phase washed with dichloromethane (3×30 mL)
  4. extractionthe resulting mixture extracted with ethyl acetate (3×50 mL)
  5. dry with materialThe combined ethyl acetate extracts were dried (Na2SO4)
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-ae96c8d7b03a4c9d8cb11f8d2ac0841b
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06939871B2

反応ノート

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