951163-61-4 Usage
Description
Carbamic acid, N-[(3S,5S)-5-methyl-3-piperidinyl]-, 1,1-dimethylethyl ester, also known as tert-Butyl ((3S,5S)-5-Methylpiperidin-3-yl)carbamate, is a carbamic acid ester compound with a specific stereochemistry and a methylpiperidinyl group. It is used as an intermediate in the synthesis of pyrrolopyrazinylureas, which are JAK kinase inhibitors.
Uses
Used in Pharmaceutical Industry:
Carbamic acid, N-[(3S,5S)-5-methyl-3-piperidinyl]-, 1,1-dimethylethyl ester is used as a synthetic intermediate for the preparation of pyrrolopyrazinylureas. These compounds act as JAK kinase inhibitors and are employed in the treatment of autoimmune and inflammatory diseases. By inhibiting JAK kinases, these compounds can help regulate immune responses and alleviate inflammation, making them valuable in the development of therapeutic agents for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 951163-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 951163-61:
(8*9)+(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*6)+(1*1)=164
164 % 10 = 4
So 951163-61-4 is a valid CAS Registry Number.
951163-61-4Relevant articles and documents
Preparation method of 3-substituted-5-aminopiperidine with protecting group
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Paragraph 0130; 0131; 0132; 0133; 0134; 0135, (2020/12/30)
The invention provides a preparation method of 3-substituted-5-aminopiperidine with a protecting group, and particularly provides a preparation method of 3-substituted-5-aminopiperidine with a protecting group, which has the advantages of low cost and easily available raw materials and reaction reagents.
STEREOSELECTIVE SYNTHESIS OF PIPERIDINE DERIVATIVES
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Page/Page column 13-14, (2010/06/22)
This invention relates to dialdehyde or dinitrile compounds, which are useful for stereoselective synthesis of piperidine, pyrrolidine, and azepane derivatives.
Coupling process for preparing quinolone intermediates
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Page/Page column 4; 5-6, (2008/06/13)
Process for making 7-cycloamino-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acids. Borate ester compounds suitable for use in such process.