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Dimethylamine → 3-[4-chloro-2-fluoro-5-(phenylmethoxy)-phenyl]-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)-dione

HRID 1450167
ノート
印刷プレビュー

反応式

HRID 1450167 の反応式
C(O[C:4]([N:6]([CH3:12])[C:7]([NH:10]C)=[N:8][CH3:9])=[O:5])C.[Cl:13][C:14]1[C:19]([O:20]CC2C=CC=CC=2)=[CH:18][C:17]([N:28]=[C:29]=[O:30])=[C:16]([F:31])[CH:15]=1.[CH3:32]NC.[C:35]1([CH3:41])[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>C[O-].[Na+]>[Cl:13][C:14]1[C:19]([O:20][CH2:41][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)=[CH:18][C:17]([N:28]2[C:29](=[O:30])[N:10]=[C:7]([N:8]([CH3:32])[CH3:9])[N:6]([CH3:12])[C:4]2=[O:5])=[C:16]([F:31])[CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 674DimethylamineHCID 1140Toluene4 回HCID 199752544-Chloro-2-fluoro-5-(phenylmethoxy)phenyl isocyanateHCID 45122948N-ethoxycarbonyl-N,N', N"-trimethylguanidine

生成物 1

HCID 199752643-[4-chloro-2-fluoro-5-(phenylmethoxy)-phenyl]-6-(dimethylamino)-1-methyl-1,3,5-triazine-2,4(1H,3H)-dione

試薬・触媒・溶媒 1

HCID 10942334
Sodium Methoxide
触媒

実験手順

To a solution of 5.05 g (29.2 mmol) of N-ethoxycarbonyl-N,N', N"-trimethylguanidine in 25 mL of toluene was added a solution of 7.72 g (27.8 mmol) of 4-chloro-2-fluoro-5-(phenylmethoxy)phenyl isocyanate in 50 mL of toluene over a period of 30 min while maintaining the temperature between 55° C. and 80° C. It was then stirred at the same temperature for an hour. To a solution of the resulting N-[N-[4-chloro-2-fluoro-5-(phenylmethoxy) phenyl]carbamoyl-N',N'-dimethylamidino]-N-methylcarbamate in toluene was added 3.21 g (71.5 mmol) of dimethylamine in 10 mL of toluene at room temperature. While the temperature was between 25° C. and 40° C., 45 mg (0.834 mmol) of sodium methoxide was added. After 30 min, it was quenched with 100 mL of water. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with 0.1N hydrochloric acid, brine, and water, dried (MgSO4) and concentrated in vacuo. The crude product was flash chromatographed over silica gel eluting with a 1:1 v:v mixture of ethyl acetate and hexane to give 5.3 g of the title compound as a brown solid, m.p.: 193°-194° C.; 1H-NMR (CDCl3, 200 MHZ) ppm 7.4 (m, 6H), 6.95 (d, 1H), 5.05 (d, 2H), 3.45 (s, 3H), 3.1 (s, 6H).

後処理

  1. temperaturewhile maintaining the temperature between 55° C. and 80° C
  2. customwas between 25° C. and 40° C.
  3. customit was quenched with 100 mL of water
  4. extractionThe aqueous layer was extracted with ethyl acetate
  5. washThe combined organic layers were washed with 0.1N hydrochloric acid, brine, and water
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customchromatographed over silica gel eluting with a 1:1 v
  9. additionv mixture of ethyl acetate and hexane

出典と根拠

ORDレコード
ord-0dd4c6ba757a4f4eb296ba3f8406f796
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05602077

反応ノート

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