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CAS No. : | 2389-45-9 | MDL No. : | MFCD00065584 |
Formula : | C19H28N2O6 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | BDHUTRNYBGWPBL-HNNXBMFYSA-N |
M.W : | 380.44 | Pubchem ID : | 2724765 |
Synonyms : |
|
Chemical Name : | Boc-Lys(Z)-OH |
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92.1% | With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; at 20℃;Industry scale; | Step 1: Preparation of Compound 1-3A mixture of compound 1-1 (1665 g, 4.379 mol, 1.0 eq), compound 1-2 (817 g, 4.51 mol, 1.03 eq), and HOBt (651 g, 4.82 mol, 1.1 eq) in 14.0 L of DCM was treated with NMM (885 g, 8.76 mol, 2.0 eq), followed by a portion wise addition of EDAC (923 g, 4.82 mol, 1.10 eq). The reaction was run at 20 C. and the reaction progress was monitored by in-process HPLC. After the reaction was completed, the reaction mixture was processed by standard extraction procedures to afford compound 1-3 (2192 g, 92.1% yield). An HPLC analysis showed the purity of compound 1-3 was 97-98%. A chiral HPLC method showed that the enantiomeric purity of compound 1-3 is was maintained (from compound 1-1) during Step 1. No undesired enantiomer was detected. |
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