Lithium Hydroxide → N-Boc-Tyr(Bn)-Leu-OH

HRID 2074350Notes

Reaction equation

HRID 2074350 reaction equation
[NH:1]([C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])[C@H:2]([C:18]([NH:20][C@H:21]([C:26]([O:28]C)=[O:27])[CH2:22][CH:23]([CH3:25])[CH3:24])=[O:19])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=1.[Li+].[OH-]>C1COCC1>[NH:1]([C:30]([O:32][C:33]([CH3:35])([CH3:34])[CH3:36])=[O:31])[C@H:2]([C:18]([NH:20][C@H:21]([C:26]([OH:28])=[O:27])[CH2:22][CH:23]([CH3:25])[CH3:24])=[O:19])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:6][CH:5]=1

Participants

4

Reactant 2

HCID 3939Lithium HydroxideHCID 11283399Boc-Tyr(Bzl)-Leu-OMe

Product 1

HCID 57611771N-Boc-Tyr(Bn)-Leu-OH

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Same procedure as above with N-Boc-Tyr(Bn)-Leu-OMe (1.034 g, 2.073 mmol), aqueous LiOH (1 M, 2.2 mL, 2.2 mmol) in THF (15 mL). A white solid was obtained (1.035 g, 100%) which was used in the next step without further purification. 1H NMR (300 MHz, CDCl3) δ 0.90 (d, J=5 Hz, 1H, Me2 Leu), 1.40 (s, 9H, (CH3)3), 1.60 (m, 3H, CH2—CH Leu), 3.00 (m, 2H, CH2), 4.29 (m, 1H, CHα), 4.44 (m, 1H, CHα), 4.88 (s, 2H, CH2 (Bn)), 5.29 (broad s, 1H, NHBoc), 6.70 (m, 1H, NH amide), 6.91 (d, J=5 Hz, 2 aromatic H), 7.12 (d, J=5 Hz, 2 aromatic H), 7.33-7.44 (m, 5 aromatic H). 3C NMR (75 MHz, CDCl3) δ 21.8, 22.9, 24.7 (CH-Me2 Leu), 28.2 ((CH3)3), 37.0 CH2 Leu), 41.1 (CH2 Tyr), 51.6 (CHα Leu), 55.7 (CHα Tyr), 70 (CH2 (Bn)), 80.4 (C(CH3)3), 114.9, 127.5, 127.9, 128.5, 128.9, 130.5, 137.0 (11 aromatic C), 155.8, 157.8 (Car-O, CO carbamate), 172.0, 176.8 (CO acid, CO amide).

Workup

  1. customA white solid was obtained (1.035 g, 100%) which
  2. customwas used in the next step without further purification

Sources & evidence

ORD record
ord-dc946ba0ec624df2b40f29c6ddf6ed62
Source dataset
uspto-grants-2011_04
Patent number
US07919468B2

Reaction notes

Loading…