Triethylamine → 6-chloro-5-fluoro-2-(methylthio)-N-(1,3-thiazol-2-ylmethyl)-4-pyrimidinamine

HRID 1366632ノート

反応式

HRID 1366632 の反応式
Cl[C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([S:10][CH3:11])[N:3]=1.Cl.[S:13]1[CH:17]=[CH:16][N:15]=[C:14]1[CH2:18][NH2:19].C(N(CC)CC)C>C1COCC1.O>[Cl:9][C:6]1[N:5]=[C:4]([S:10][CH3:11])[N:3]=[C:2]([NH:19][CH2:18][C:14]2[S:13][CH:17]=[CH:16][N:15]=2)[C:7]=1[F:8]

参加物

6

反応物 3

HCID 8471TriethylamineHCID 223782774,6-Dichloro-5-fluoro-2-(methylsulfanyl)pyrimidine2 回HCID 42614216(1,3-Thiazol-2-yl)methanamine hydrochloride

生成物 1

HCID 866370136-chloro-5-fluoro-2-(methylthio)-N-(1,3-thiazol-2-ylmethyl)-4-pyrimidinamine収率 117%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

4,6-Dichloro-5-fluoro-2-(methylthio)pyrimidine (see Intermediate E) (0.422 g, 1.991 mmol), commercially available (1,3-thiazol-2-ylmethyl)amine hydrochloride (0.300 g, 1.992 mmol) and triethylamine (0.61 mL, 4.3765 mmol) were dissolved in THF (3 mL) and left to stir for 4 days. The reaction mixture was diluted with water, and the aqueous layer was extracted with ethyl acetate. The organics were dried (MgSO4) and concentrated to produce 6-chloro-5-fluoro-2-(methylthio)-N-(1,3-thiazol-2-ylmethyl)-4-pyrimidinamine as a yellow-orange solid (0.6773 g). LCMS: (M+H)+=291.0.

後処理

  1. waitleft
  2. extractionthe aqueous layer was extracted with ethyl acetate
  3. dry with materialThe organics were dried (MgSO4)
  4. concentrationconcentrated

出典と根拠

ORDレコード
ord-ee6c2258b3374310824c472e832215c2
出典データセット
uspto-grants-2011_02
特許番号
US07893056B2

反応ノート

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