Alternatived Products of [ 3886-08-6 ]
Product Details of [ 3886-08-6 ]
CAS No. : | 3886-08-6 |
MDL No. : | MFCD00038274 |
Formula : |
C17H23NO6
|
Boiling Point : |
- |
Linear Structure Formula : | C6H5CH2OCONHCH(CH2CH2COOC(CH3)3)COOH |
InChI Key : | GLMODRZPPBZPPB-ZDUSSCGKSA-N |
M.W : |
337.37
|
Pubchem ID : | 107472 |
Synonyms : |
|
Chemical Name : | (S)-2-(((Benzyloxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid |
Application In Synthesis of [ 3886-08-6 ]
* 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 [ 3886-08-6 ]
- 1
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[ 3886-08-6 ]
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[ 53838-27-0 ]
- 2
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[ 3886-08-6 ]
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[ 220303-63-9 ]
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[ 53838-27-0 ]
Yield | Reaction Conditions | Operation in experiment |
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|
Preparative Example C Synthesis of N-(Toluene-4-sulfonyl)-L-prolyl-D-glutamic acid N-Benzyloxycarbonyl-D-5-(1,1-dimethylethyl)-glutamic acid was converted to the methyl ester using the procedure described in Method 2. D-5-(1,1-dimethylethyl)-glutamic acid methyl ester was prepared from the product of the previous step utilizing the procedure described in Method 4. N-(Toluene-4-sulfonyl)-L-proline hydrate was coupled to the resulting D-5-(1,1-dimethylethyl)-glutamic acid methyl ester utilizing the procedure described in Method 3. The methyl ester was hydrolyzed using the procedure described in Method 6. The product was isolated as a white solid, mp=50 C. The title compound was then prepared using the procedure described in Method 11. The product as isolated as a white solid, mp=60 C. NMR data was as follows: 1H NMR (DMSO-d6, 300 MHz):δ=8.12 (d, 1 H, J=4.0 Hz); 7.73 (m, 2 H); 7.43, (m, 2 H); 4.25 (m, 1 H); 4.05 (m, 1 H); 3.43 (m, 1 H); 3.15 (m, 1 H); 2.40 (s, 3 H), 2.45 (m, 2 H); 2.02 (m, 2 H); 1.90-1.40 (bm, 4 H). |
- 3
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[ 29022-11-5 ]
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[ 35661-60-0 ]
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[ 3886-08-6 ]
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[ 122889-11-6 ]
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[ 71989-31-6 ]
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[ 71989-38-3 ]
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2-chlorotrityl resin
[ No CAS ]
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Cbz-E(OtBu)PLGS(OBn)Y(OtBu)L-COOH
[ No CAS ]