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Chemical Structure| 96702-03-3 Chemical Structure| 96702-03-3
Chemical Structure| 96702-03-3

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Ectoine induced salt tolerance

Synonyms: Ectoin; THP(B); Pyrostatin B

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of Ectoine

CAS No. :96702-03-3
Formula : C6H10N2O2
M.W : 142.16
SMILES Code : O=C([C@H]1NC(C)=NCC1)O
Synonyms :
Ectoin; THP(B); Pyrostatin B
English Name :(S)-2-Methyl-3,4,5,6-tetrahydropyrimidine-4-carboxylic acid
MDL No. :MFCD03419286
InChI Key :WQXNXVUDBPYKBA-YFKPBYRVSA-N
Pubchem ID :126041

Safety of Ectoine

Application In Synthesis of Ectoine

* 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 [ 96702-03-3 ]

[ 96702-03-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 15471-17-7 ]
  • [ 96702-03-3 ]
  • 1-(3-sulfopropyl)pyridinium 2-methyl-3,4,5,6-tetrahydropyrimidine-4-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water; at 20 - 60℃; for 1.0h; Example 4 1-(3-Sulfopropyl)pyridinium 2-methyl-3,4,5,6-tetrahydropyrimidine-4-carboxylate 35.26 g of ectoin are dissolved in 50 ml of water in a 250 ml beaker, and 50 g of 3-pyridinopropane-1-sulfonate are subsequently added at room temperature with stirring. This reaction solution is stirred at room temperature for a further hour and subsequently evaporated to dryness in a rotary evaporator with a water bath at about 60 C., leaving a white solid.
  • 2
  • [ 1445-45-0 ]
  • [ 1758-80-1 ]
  • [ 96702-03-3 ]
YieldReaction ConditionsOperation in experiment
72 % With triethylamine In methanol at 65℃; 1.4; 2-6; 10 (4) Preparation of (S) -1,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid After connecting a condenser to a 500mL two-neck round flask and circulating the refrigerant, 11.81g of (S)-2,4-diaminobutanoic acid, 10.2g of triethylamine, 120mL of methanol and 24.1g of trimethylorthoacetate prepared above was added and stirred under reflux at 65° C. for 12 hours to perform a cyclization reaction.Next, the completion of the reaction was confirmed by TLC, the reaction solution was cooled to room temperature (23-25 ° C), and then concentrated under reduced pressure to remove the solvent.50 mL of methanol and 110 mL of ethyl acetate were added to the residue, stirred at room temperature (20 to 25 ° C) for 2 hours, and then filtered to obtain 10.24 g of ectoin (72% yield) as the final target compound.In addition, the obtained ectoin was analyzed by liquid chromatography to confirm that the purity was 99.3%.
72 % With triethylamine In methanol at 65℃; 1.4; 2-6; 8-9 (4) Preparation of (S)-1,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid After connecting the condenser to a 500 mL two-necked round flask and circulating the refrigerant, 11.81 g of (S)-2,4-diaminobutanoic acid, 10.2 g of triethylamine, 120 mL of methanol, and 24.1 g of trimethyl orthoacetate prepared previously were added. was added and refluxed and stirred at 65°C for 12 hours to perform a cyclization reaction.Next, completion of the reaction was confirmed by TLC, the reaction solution was cooled to room temperature (23-25°C), and the solvent was removed by concentration under reduced pressure.50 mL of methanol and 110 mL of ethyl acetate were added to the residue, stirred for 2 hours at room temperature (20 ~ 25°C), and then filtered to obtain 10.24 g (72% yield) of heterocyclic amino acid, the final target compound.In addition, the obtained heterocyclic amino acid was analyzed by liquid chromatography and confirmed to be 99.9% pure.
72 % In butan-1-ol Reflux; 4-5 [Example 4] Preparation of ectoine-1 A condenser was connected to a 500 mL two-necked round bottom flask, and the refrigerant was circulated. Then, 11.81 g of the above (S)-2,4-diaminobutanoic acid, 120 mL of n-butanol, and 24.1 g of trimethylorthoacetate were added and stirred under reflux for 12 hours. Next, the completion of the reaction was confirmed by TLC, and the reaction solution was cooled to room temperature and concentrated under reduced pressure to remove the solvent. 50 mL of methanol and 100 mL of ethyl acetate were added to the residue, stirred at room temperature for 2 hours, and then filtered to finally obtain 10.24 g of ectoine (yield 72%). In addition, the purity of the obtained ectoine was confirmed to be 99.3% by analyzing it by liquid chromatography,
 

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