1-(Methoxymethyl)-6-phenylthiothymine → 5-Methyl-6-phenyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-4-one

HRID 1057246

反応式

HRID 1057246 の反応式
COC[N:4]1[C:12]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:10]([CH3:11])[C:8](=[O:9])[NH:7][C:5]1=[S:6]>Cl>[C:13]1([C:12]2[NH:4][C:5](=[S:6])[NH:7][C:8](=[O:9])[C:10]=2[CH3:11])[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

参加物

3

反応物 1

HCID 540163721-(Methoxymethyl)-6-phenylthiothymine

生成物 1

HCID 186710275-Methyl-6-phenyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-4-one収率 28.1%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

To 100 ml of concentrated hydrochloric acid, 17.2 g (62 mmole) of 1-(methoxymethyl)-6-phenylthiothymine was added and allowed to react for 2 hours at 80° C. The reaction mixture was concentrated under reduced pressure and crystallized from ethanol to obtain 3.8 g of the target compound (Yield: 26%).

後処理

  1. customto react for 2 hours at 80° C
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customcrystallized from ethanol

出典と根拠

ORDレコード
ord-056e0b3594f941d2bdc595bec5ef86f0
出典データセット
uspto-grants-2003_02
特許番号
USRE037979E1

関連ノート

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