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

HRID 1484096노트

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HRID 1484096 반응식
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]

참가 물질

5

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f98186162f1f47d496c5e094dadc2f21
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09421237B2

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