m-Chloroperbenzoic acid → 4'-(Cyclopropylmethyl)-2-(methylsulfinyl)-4,5'-bipyrimidine

HRID 1397136ノート

反応式

HRID 1397136 の反応式
[CH:1]1([CH2:4][C:5]2[C:10]([C:11]3[CH:16]=[CH:15][N:14]=[C:13]([S:17][CH3:18])[N:12]=3)=[CH:9][N:8]=[CH:7][N:6]=2)[CH2:3][CH2:2]1.C1C=C(Cl)C=C(C(OO)=[O:27])C=1>C(Cl)Cl>[CH:1]1([CH2:4][C:5]2[C:10]([C:11]3[CH:16]=[CH:15][N:14]=[C:13]([S:17]([CH3:18])=[O:27])[N:12]=3)=[CH:9][N:8]=[CH:7][N:6]=2)[CH2:2][CH2:3]1

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 679837614'-(Cyclopropylmethyl)-2-(methylsulfanyl)-4,5'-bipyrimidine

生成物 1

HCID 679831774'-(Cyclopropylmethyl)-2-(methylsulfinyl)-4,5'-bipyrimidine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 4′-(cyclopropylmethyl)-2-(methylsulfanyl)-4,5′-bipyrimidine (4a) (62.5 mg, 0.242 mmol) in DCM (968 μl), mCPBA (65.1 mg, 0.290 mmol) was added and the reaction mixture was stirred at rt for 1 hour. The crude reaction mixture was partitioned between saturated sodium bicarbonate solution and DCM. The aqueous layer was separated and back-extracted twice with DCM. The combined organic extracts were washed with brine, dried over sodium sulfate, then concentrated in vacuo. The crude product was carried on to the next step without further purification. MS (ES+): m/z=275.2 (100) [MH+]. HPLC: tR=0.72 minute over 3 minutes. Purity: 100% [HPLC (LC/MS) at 220 nm].

後処理

  1. customThe crude reaction mixture
  2. customwas partitioned between saturated sodium bicarbonate solution and DCM
  3. customThe aqueous layer was separated
  4. extractionback-extracted twice with DCM
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe crude product was carried on to the next step without further purification
  9. waitHPLC: tR=0.72 minute over 3 minutes

出典と根拠

ORDレコード
ord-354d53a64e894d7b920454679594783d
出典データセット
uspto-grants-2014_12
特許番号
US08901147B2

反応ノート

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