Trifluoroacetic acid → HCID 131726067, compound

HRID 722831Notes

Reaction equation

HRID 722831 reaction equation
[NH:1]([C:77]([O:79][C:80]([CH3:83])([CH3:82])[CH3:81])=[O:78])[CH2:2][C:3]([NH:5][C@H:6]([C:13]([NH:15][C@H:16]([C:38]([NH:40][C@H:41]([C:49]([NH:51][C@H:52]([C:57]([NH:59][C@H:60]([C:67]([N:69]1[CH2:76][CH2:75][CH2:74][C@H:70]1[C:71]([OH:73])=[O:72])=[O:68])[CH2:61][O:62][C:63]([CH3:66])([CH3:65])[CH3:64])=[O:58])[CH2:53][CH:54]([CH3:56])[CH3:55])=[O:50])[CH2:42][C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)=[O:39])[CH2:17][O:18]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:14])[CH2:7][O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:4].C1C=CC(C(Cl)(C2C(Cl)=CC=CC=2)C2C=CC=CC=2)=CC=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.N1CCCCC1.N(C(OC(C)(C)C)=O)CC(O)=O.C(O)(C(F)(F)F)=O>>[NH:1]([C:77]([O:79][C:80]([CH3:81])([CH3:82])[CH3:83])=[O:78])[CH2:2][C:3]([NH:5][C@H:6]([C:13]([NH:15][C@H:16]([C:38]([NH:40][C@H:41]([C:49]([NH:51][C@H:52]([C:57]([NH:59][C@H:60]([C:67]([N:69]1[CH2:76][CH2:75][CH2:74][C@H:70]1[C:71]([OH:73])=[O:72])=[O:68])[CH2:61][O:62][C:63]([CH3:64])([CH3:65])[CH3:66])=[O:58])[CH2:53][CH:54]([CH3:55])[CH3:56])=[O:50])[CH2:42][C:43]1[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=1)=[O:39])[CH2:17][OH:18])=[O:14])[CH2:7][O:8][C:9]([CH3:10])([CH3:11])[CH3:12])=[O:4]

Participants

6

Reactant 5

HCID 6422Trifluoroacetic acidHCID 8082PiperidineHCID 78288N-(tert-butoxycarbonyl)glycineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 131726068HCID 131726068, compound

Product 1

HCID 131726067HCID 131726067, compound

Procedure

A Boc-Gly-Ser(tBu)-Ser(Trt)-Phe-Leu-Ser(tBu)-Pro-2-chlorotrityl resin was constructed on a prolyl-2-chlorotrityl resin (466 mg, 0.25 mmol, manufactured by Novabiochem) by repeating successively introduction of Fmoc-amino acid with HBTU and de-Fmoc with piperidine to introduce Boc-Gly into a N-terminal residue using a peptide automatic synthesizer. This resin was treated with 1% TFA, 5% TIPS/dichloromethane for 30 minutes, to perform removal of a Trt group and cleavage from the resin at the same time. After the resin was filtered, dichloromethane was distilled off under reduced pressure to concentrate the material, and Et2O was added to obtain precipitates, which were dried to obtain 165 mg of Boc-Gly-Ser(tBu)-Ser-Phe-Leu-Ser(tBu)-Pro-OH as white precipitates. Then, phenacyl bromide (40 mg, 1.1 equivalents) and triethylamine (20 mg, 1.1 equivalents) were added to react them for 2 hours in about 3 mL of DMF. After the reaction, the reaction solution was placed into an about 5-fold amount of ethyl acetate, and the mixture was washed with water and an aqueous saturated sodium chloride solution, dried over sodium sulfate, filtered, and concentrated. The precipitates formed upon addition of Et2O were dried to obtain Boc-Gly-Ser(tBu)-Ser-Phe-Leu-Ser(tBu)-Pro-OPac as white precipitates. Then, octanoic acid (18.2 mg, 1.1 equivalents), EDC.HCl (26.4 mg, 1.2 equivalents) and DMAP (1.4 mg, 0.1 equivalent) were added to react them overnight in about 2 mL of DMF. The reaction solution was placed into an about 5-fold amount of ethyl acetate, washed with water and an aqueous saturated sodium chloride solution, sodium sulfate was added to dry it, and this was filtered, concentrated, Et2O was added to obtain 144 mg of Boc-Gly-Ser(tBu)-Ser(Octanoyl)-Phe-Leu-Ser(tBu)-Pro-OPac as white precipitates. Then, 1.5 mL of acetic acid and zinc powder (163 mg, 20 equivalents) were added to react them for 1 hour, this was filtered, and cold water was added to obtain precipitates, which were washed with Et2O and dried. 65 mg of Boc-Gly-Ser(tBu)-Ser(Octanoyl)-Phe-Leu-Ser(tBu)-Pro-OH was obtained as white precipitates. The product was dissolved in about 2 mL of a mixed solution of aqueous acetic acid and acetonitrile, the solution was added to YMC-Pack ODS-A (20 mm×250 mm), and this was eluted with a linear gradient (flow rate: 10 mL/min) of acetonitrile 40% to 80% in 0.1% trifluoroacetic acid for 60 minutes. The desired fractions were taken, and lyophilized to obtain 50 mg of the desired product.

Workup

  1. customremoval of a Trt group and cleavage from the resin at the same time
  2. filtrationAfter the resin was filtered
  3. distillationdichloromethane was distilled off under reduced pressure
  4. concentrationto concentrate the material, and Et2O
  5. additionwas added
  6. customto obtain
  7. customprecipitates
  8. customwhich were dried

Sources & evidence

ORD record
ord-cedb32ae5fd4495c91b18ba274e9961a
Source dataset
uspto-grants-2006_11
Patent number
US07138489B2

Reaction notes

Loading…