Methyl iodide → 2-Amino-4-(3,5-diacetylphenyl)amino-1,6-dimethylpyrimidinium iodide

HRID 1071456

반응식

HRID 1071456 반응식
[NH2:1][C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:14]=[C:13]([C:15](=[O:17])[CH3:16])[CH:12]=[C:11]([C:18](=[O:20])[CH3:19])[CH:10]=2)[CH:5]=[C:4]([CH3:21])[N:3]=1.[CH3:22][I:23]>C(#N)C.O1CCCC1>[I-:23].[NH2:1][C:2]1[N:7]=[C:6]([NH:8][C:9]2[CH:10]=[C:11]([C:18](=[O:20])[CH3:19])[CH:12]=[C:13]([C:15](=[O:17])[CH3:16])[CH:14]=2)[CH:5]=[C:4]([CH3:21])[N+:3]=1[CH3:22]

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 133109Cni H1194

생성물 1

HCID 98453522-Amino-4-(3,5-diacetylphenyl)amino-1,6-dimethylpyrimidinium iodide

시약·촉매·용매 1

HCID 22177404Acetonitrile tetrahydrofuran용매

반응 조건

온도
42.5 °C

실험 절차

Compound No. 2, FIG. 1A: A suspension of Compound No. 11 (2-amino-4-(3,5-diacetylphenyl)amino-6-methylpyrimidine) (0.284 g), was suspended in 1:1 acetonitrile-tetrahydrofuran was treated with methyl iodide (2 mL) and heated at 40-45° C. under a reflux condenser for 18 hr. Cooling and filtration gave 0.35 g of 2-amino-4-(3,5-diacetylphenyl)amino-1,6-dimethylpyrimidinium iodide, mp 292° C.

후처리

  1. addition2, FIG. 1A: A suspension of Compound No
  2. temperatureCooling
  3. filtrationfiltration

출처 및 근거

ORD 기록
ord-40383a42c2e5457a9a7c5c1d5a3ebfc2
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06906076B2

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