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Chemical Structure| 13518-40-6 Chemical Structure| 13518-40-6
Chemical Structure| 13518-40-6

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H-Val-OtBu·HCl is a valine derivative, commonly used in peptide synthesis and drug development.

Synonyms: tert-Butyl (S)-2-amino-3-methylbutanoate hydrochloride; tert-Butyl L-valinate hydrochloride

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Product Details of H-Val-OtBu·HCl

CAS No. :13518-40-6
Formula : C9H20ClNO2
M.W : 209.71
SMILES Code : N[C@@H](C(C)C)C(OC(C)(C)C)=O.[H]Cl
Synonyms :
tert-Butyl (S)-2-amino-3-methylbutanoate hydrochloride; tert-Butyl L-valinate hydrochloride
MDL No. :MFCD00034863
InChI Key :AUIVQIHTTVPKFS-FJXQXJEOSA-N
Pubchem ID :12490702

Safety of H-Val-OtBu·HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of H-Val-OtBu·HCl

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 13518-40-6 ]

[ 13518-40-6 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 13518-40-6 ]
  • [ 27486-87-9 ]
  • (S)-2-((R)-2-Acetylamino-3-tritylsulfanyl-propionylamino)-3-methyl-butyric acid tert-butyl ester [ No CAS ]
  • 2
  • [ 97-08-5 ]
  • [ 13518-40-6 ]
  • [ 873923-16-1 ]
  • 3
  • [ 858103-94-3 ]
  • [ 91183-71-0 ]
  • [ 13518-40-6 ]
  • C39H45F2N3O7S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 55; N-[4-((2R, 3R)-1-(4-fluorophenyl)-3-[2-(4-fluorophenyl)-2-hydroxyethyl] thio}-4- oxoazetidin-2-yl) phenoxy] acetyl}-D-valyl-L-methionine; N-[4-((2R,3R)-1-(4-Fluorophenyl)-3-[2-(4-fluorophenyl)-2-oxoethyl]thio}-4-oxoazetidin-2- yl) phenoxy] acetyl}-D-valine (13.3 mg, 0.023 mmol), tert-butyl L-methioninate hydrochloride (7.4 mg, 0.031 mmol) and N-methylmorpholine (10, ul, 0.091 mmol) were dissolved in 1 ml. After 5 minutes, TBTU (8.9 mg, 0.028 mmol) was added and the resulting suspension was stirred overnight. Additional tert-butyl L-methioninate hydrochloride (2.1 mg, 0087 mmol), N-methylmorpholine (5, ul, 45, umol) and TBTU (2.1 mg, 6.54 jumol) were added and the mixture was stirred for 2 h. The formation of the ester was confirmed. M/z 768.1 (M-H) and 770.0 (M+H). The yellow suspension was purified on silica gel (1g) and eluted with EtOAc: DCM (15: 85). The pure fractions were concentrated and formic acid (1.5 ml) was added. The solution was stirred at 50C overnight. The solvent was removed under reduced pressure. Toluene was added and removed under reduced pressure. The residue was dissolved in methanol (1 ml) and sodium borohydride (9.9 mg, 0.26 mmol) was added. The resulting reaction mixture was stirred for 10 minutes. Ammonium acetate (18.9 mg) was added and the solvent was removed under reduced pressure. The residue was purified with preparative HPLC on a C8 column. A gradient from 20% to 40 % MeCN in 0.1 M ammonium acetate buffer was used as eluent. After lyophilisation, the title compound was obtained as a white solid was obtained (4.6 mg, 28%). 1H-NMR (400 MHz, DMSO-d6) : 0.75 (d, 3H), 0.79 (d, 3H), 1.79-1. 97 (m, 3H), 1.99 (s, 3H), 2.36-2. 44 (m, 2H), 2.86-2. 92 (m, 2H), 2.24-4. 35 (m, 3H), 4.58 (d, 2H), 4.67-4. 76 (m, 1H), 5.03 (d, 0.5H), 5.5 (d, 0. 5H), 5.63 (t, 1H), 6.95 (d, 2H), 7.05-7. 16 (m, 4H), 7.18-7. 24 (m, 2H), 7.30-7. 38 (m, 2H), 7.82 (d, 1H), 7.37 (d, 1H). M/z : 714.0 (M-1) and 716.1 (M+H).
  • 4
  • [ 13518-40-6 ]
  • [ 193954-26-6 ]
  • Fmoc-L-β-HoAla-L-Val-O-t-Bu [ No CAS ]
 

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