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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
881310-04-9

(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate synthesis

5synthesis methods
59936-29-7 Synthesis
Boc-L-Proline-methyl ester

59936-29-7
233 suppliers
$6.00/5g

(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

881310-04-9
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Yield:881310-04-9 87%

Reaction Conditions:

with hydrazine hydrate at 20;Reflux;

References:

Jansen, Michaela;Rabe, Holger;Strehle, Axelle;Dieler, Sandra;Debus, Fabian;Dannhardt, Gerd;Akabas, Myles H.;Lüddens, Hartmut [Journal of Medicinal Chemistry,2008,vol. 51,# 15,p. 4430 - 4448] Location in patent:supporting information; experimental part

1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, 2-[2-[(phenylmethoxy)carbonyl]hydrazide], (2S)-

122588-88-9
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(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

881310-04-9
21 suppliers
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References
BOC-L-Proline

15761-39-4
616 suppliers
$5.00/10g

(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

881310-04-9
21 suppliers
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References
147-85-3 Synthesis
L-Proline

147-85-3
1033 suppliers
$6.00/25g

(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

881310-04-9
21 suppliers
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References
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
863 suppliers
$13.50/25G

(S)-tert-Butyl 2-(hydrazinecarbonyl)pyrrolidine-1-carboxylate

881310-04-9
21 suppliers
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References

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