Hydrochloric Acid → (Pyrazine-2-carbonyl)-L-phenylalanyl-L-phenylalanine

HRID 1484096ノート

反応式

HRID 1484096 の反応式
C[O:2][C:3](=[O:32])[C@H:4]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[NH:5][C:6](=[O:24])[C@H:7]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[NH:8][C:9]([C:11]1[CH:16]=[N:15][CH:14]=[CH:13][N:12]=1)=[O:10].[OH-].[Na+].Cl>CC(C)=O>[N:12]1[CH:13]=[CH:14][N:15]=[CH:16][C:11]=1[C:9]([NH:8][C@H:7]([C:6]([NH:5][C@H:4]([C:3]([OH:32])=[O:2])[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:24])[CH2:17][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)=[O:10]

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 67285910HCID 67285910、化合物

生成物 1

HCID 67286253(Pyrazine-2-carbonyl)-L-phenylalanyl-L-phenylalanine収率 90.5%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

The product of N-pyrazineformyl-L-phenylalanyl-L-phenylalanine methyl ester (1.52 g, 3.52 mmol) in Preparation example 4 was dissolved with 10 ml of acetone, 2N NaOH was added dropwise slowly under the condition of ice water bath until a pH value of 12˜13 was obtained, and the solution was kept reacting under the condition of an ice water bath, the reaction was monitored by TLC and completed after 2 h. Hydrochloric acid was added dropwise under the condition of ice water bath until a pH value of 2˜3 was obtained, a large amount of white solid was produced, the generated precipitate was filtered, washed with diethyl ether followed by airing to dry, 1.33 g of white product was obtained with a yield of 90.5%, the melting point of the white solid: 194-196° C.; 1H-NMR (DMSO-d6, 300 MHz): δ 12.88 (s, 1H), 9.10 (s, 1H), 8.90-8.87 (m, 1H), 8.77-8.73 (m, 1H), 8.75-8.65 (m, 2H), 7.24-7.14 (m, 10H), 4.84-4.80 (m, 1H), 4.53-4.50 (m, 1H), 3.14-2.89 (m, 4H).

後処理

  1. additionwas added dropwise slowly under the condition of ice water bath until a pH value of 12˜13
  2. customwas obtained
  3. customthe solution was kept reacting under the condition of an ice water bath
  4. customwas obtained
  5. customa large amount of white solid was produced
  6. filtrationthe generated precipitate was filtered
  7. washwashed with diethyl ether
  8. customto dry

出典と根拠

ORDレコード
ord-f98186162f1f47d496c5e094dadc2f21
出典データセット
uspto-grants-2016_08
特許番号
US09421237B2

反応ノート

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