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Formic Acid → Boc-Leu-Leu-Lys(Z)-Leu-Leu-OH

HRID 2298449
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인쇄 미리보기

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HRID 2298449 반응식
[OH-].[Na+].[NH:3]([C:56]([O:58][C:59]([CH3:62])([CH3:61])[CH3:60])=[O:57])[C@H:4]([C:9]([NH:11][C@H:12]([C:17]([NH:19][C@H:20]([C:36]([NH:38][C@H:39]([C:44]([NH:46][C@H:47]([C:52]([O:54]C)=[O:53])[CH2:48][CH:49]([CH3:51])[CH3:50])=[O:45])[CH2:40][CH:41]([CH3:43])[CH3:42])=[O:37])[CH2:21][CH2:22][CH2:23][CH2:24][NH:25][C:26]([O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:27])=[O:18])[CH2:13][CH:14]([CH3:16])[CH3:15])=[O:10])[CH2:5][CH:6]([CH3:8])[CH3:7].C1COCC1.C(O)=O>O.C(OCC)(=O)C>[NH:3]([C:56]([O:58][C:59]([CH3:62])([CH3:61])[CH3:60])=[O:57])[C@H:4]([C:9]([NH:11][C@H:12]([C:17]([NH:19][C@H:20]([C:36]([NH:38][C@H:39]([C:44]([NH:46][C@H:47]([C:52]([OH:54])=[O:53])[CH2:48][CH:49]([CH3:50])[CH3:51])=[O:45])[CH2:40][CH:41]([CH3:42])[CH3:43])=[O:37])[CH2:21][CH2:22][CH2:23][CH2:24][NH:25][C:26]([O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:27])=[O:18])[CH2:13][CH:14]([CH3:16])[CH3:15])=[O:10])[CH2:5][CH:6]([CH3:8])[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 284Formic AcidHCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 12020547Boc-Leu-Leu-Lys(Z)-Leu-Leu-OMe

생성물 1

HCID 12020548Boc-Leu-Leu-Lys(Z)-Leu-Leu-OH수율 97.5%

시약·촉매·용매 2

HCID 962
Water
용매
2회
HCID 8857Ethyl Acetate용매

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온도
62.5 °C

실험 절차

A solution of NaOH(1.44 g, 36.0 mmol) in H2O (15.0 g) was added at 20-25° C. over 5 min to a mixture of Boc-Leu-Leu-Lys(Z)-Leu-Leu-OMe (SEQ. ID No. 2) (12.0 g, 14.16 mmol) THF (48.0 g) and H2O (18.0 g). The resulting mixture was stirred for 2 h. 98% Formic acid (5 g) was added, followed by ethyl acetate (30.0 g). The resulting organic phase was washed with H2O, concentrated in vacuo and the residue was dissolved in MeOH (60.0 g). The solids were filtered and rinsed with an additional portion of MeOH (8.0 g). The combined MeOH solution was heated to 60-65° C. and H2O (30.0 g) was added over 10 min. This mixture was cooled to 20-25° C., the solid product began to crystallize. An additional portion of H2O (35.0 g) was added and the mixture was stirred for 1 h. The solid product was filtered, washed with H2O and dried in vacuo to give Boc-Leu-Leu-Lys(Z)-Leu-Leu-OH (SEQ. ID No. 2) (11.5 g, 97.5%).

후처리

  1. washThe resulting organic phase was washed with H2O
  2. concentrationconcentrated in vacuo
  3. dissolutionthe residue was dissolved in MeOH (60.0 g)
  4. filtrationThe solids were filtered
  5. washrinsed with an additional portion of MeOH (8.0 g)
  6. additionH2O (30.0 g) was added over 10 min
  7. temperatureThis mixture was cooled to 20-25° C.
  8. customto crystallize
  9. additionAn additional portion of H2O (35.0 g) was added
  10. stirringthe mixture was stirred for 1 h
  11. filtrationThe solid product was filtered
  12. washwashed with H2O
  13. customdried in vacuo

출처 및 근거

ORD 기록
ord-a24bf1aa912b47238f6d0e91d53a75d4
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06492490B1

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