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Potassium Carbonate → 4-(6-Cyclobutanecarbonylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole

HRID 2379887
ノート
印刷プレビュー

反応式

HRID 2379887 の反応式
[CH:1]1([C:5]([OH:7])=O)[CH2:4][CH2:3][CH2:2]1.O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.Cl.Cl.Cl.[NH2:34][CH2:35][C:36]1[N:41]=[C:40]([C:42]2[N:43]=[C:44]([N:47]=[C:48]([NH2:50])[NH2:49])[S:45][CH:46]=2)[CH:39]=[CH:38][CH:37]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.O.O1CCCC1.C(OCC)(=O)C.C(N(CC)CC)C>[CH:1]1([C:5]([NH:34][CH2:35][C:36]2[N:41]=[C:40]([C:42]3[N:43]=[C:44]([N:47]=[C:48]([NH2:50])[NH2:49])[S:45][CH:46]=3)[CH:39]=[CH:38][CH:37]=2)=[O:7])[CH2:2][CH2:3][CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 5

HCID 11430Potassium CarbonateHCID 19494Cyclobutanecarboxylic acidHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 189538374-(6-Aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole trihydrochloride

生成物 1

HCID 10042277
4-(6-Cyclobutanecarbonylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole

試薬・触媒・溶媒 4

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒2 回HCID 8471Triethylamine溶媒HCID 21939870Tetrahydrofuran ethyl acetate溶媒

実験手順

A mixture of cyclobutanecarboxylic acid (0.5 ml), 1-hydroxybenzotriazole hydrate (0.8 g) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.0 g) in N,N-dimethylformamide (5 ml) was stirred for 1 hour at ambient temperature. The above mixture was added to a mixture of 4-(6-aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole trihydrochloride (1.5 g) and triethylamine (1.8 ml) in N,N-dimethylformamide (15 ml) and the mixture was sitrred for 20 hours at ambient temperature. The reaction mixture was added a mixture of ethyl acetate tetrahydrofuran and water and the mixture was adjusted to pH 9.5 with 20% aqueous potassium carbonate. The separated organic layer was washed with brine and dried over magnesium sulfate. The solvent was removed by concentration and the residue was recrystallized from a mixture of N,N-dimethylformamide and ethyl acetate to give 4-(6-cyclobutanecarbonylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (0.86 g).

後処理

  1. waitthe mixture was sitrred for 20 hours at ambient temperature
  2. additionThe reaction mixture was added
  3. washThe separated organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed by concentration
  6. customthe residue was recrystallized from a mixture of N,N-dimethylformamide and ethyl acetate

出典と根拠

ORDレコード
ord-07832cf9745d4e0b9032086195224dc3
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05364871

反応ノート

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