Guanidine Hydrochloride → 4-(2-Chloropyridin-3-yl)pyrimidin-2-amine

HRID 1361648ノート

反応式

HRID 1361648 の反応式
[Na].Cl.[NH2:3][C:4]([NH2:6])=[NH:5].[Cl:7][C:8]1[C:13]([C:14](=O)/[CH:15]=[CH:16]/N(C)C)=[CH:12][CH:11]=[CH:10][N:9]=1>CO>[Cl:7][C:8]1[C:13]([C:14]2[CH:15]=[CH:16][N:3]=[C:4]([NH2:6])[N:5]=2)=[CH:12][CH:11]=[CH:10][N:9]=1

参加物

5

反応物 3

HCID 5742Guanidine HydrochlorideHCID 5360545SodiumHCID 161089731-(2-Chloropyridin-3-yl)-3-(dimethylamino)prop-2-en-1-one

生成物 1

HCID 533963354-(2-Chloropyridin-3-yl)pyrimidin-2-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In an argon purged 500 mL round bottom flask placed in an isopropanol bath (used as a heat sink), added sodium metal (3.40 g, 148 mmol) slowly to methanol (180 mL). Stirred at RT for 30 minutes. Added guanidine hydrochloride (17.0 g, 182 mmol), stirred at RT for 30 minutes, added (E)-1-(2-chloropyridin-3-yl)-3-(dimethylamino)prop-2-en-1-one (12.0 g, 57.0 mmol), attached air condenser, and heated to 50° C. for 24 hours. Removed approximately half of the methanol by rotary evaporation. Filtered solids onto side-armed flask under vacuum, then washed with saturated NaHCO3 and H2O, air dried to yield 4-(2-chloropyridin-3-yl)pyrimidin-2-amine as off-white solid. MS (M+H)+=206. Calc'd 206.63 for C9H7ClN4.

後処理

  1. customIn an argon purged 500 mL round bottom flask
  2. customplaced in an isopropanol bath
  3. temperatureheated to 50° C. for 24 hours
  4. customRemoved approximately half of the methanol
  5. customby rotary evaporation
  6. filtrationFiltered solids onto side-armed flask under vacuum
  7. washwashed with saturated NaHCO3 and H2O, air
  8. customdried

出典と根拠

ORDレコード
ord-cb32fd2c6dbb424c83d7847d6a162691
出典データセット
uspto-grants-2011_02
特許番号
US07880000B2

反応ノート

読み込み中…