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2-(N-t-butylamino)pyrimidine is an organic compound with the molecular formula C9H14N4. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound features a t-butylamine group (N-t-butylamino) attached to the 2-position of the pyrimidine ring, which introduces a sterically hindered alkyl group that can influence the compound's reactivity and physical properties. This chemical is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form diverse molecular structures through further chemical reactions.

2958-83-0

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2958-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2958-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2958-83:
(6*2)+(5*9)+(4*5)+(3*8)+(2*8)+(1*3)=120
120 % 10 = 0
So 2958-83-0 is a valid CAS Registry Number.

2958-83-0Relevant academic research and scientific papers

Gas-phase pyrolytic reactions of N-ethyl, N-isopropyl, and N-t-butyl substituted 2-aminopyrazine and 2-aminopyrimidine

Al-Awadi, Nouria A.,El-Dusouqui, Osman M. E.,Kaul, Kamini,Dib, Hicham H.

, p. 403 - 407 (2000)

The rates of gas-phase elimination of N-ethyl (1), N-isopropyl (2), N-t-butyl (3) substituted 2-aminopyrazine and N-ethyl (4), N-isopropyl (5), and N-t-butyl (6) substituted 2-aminopyrimidine have been measured. The compounds undergo unimolecular first-order pyrolytic reactions. The relative rates of the primary:secondary:tertiary alkyl homologues at 600 K are 1:14.4:38.0 for the pyrazines and 1:20.8:162.5 for the pyrimidines, respectively. The reactivities of these compounds have been compared with those of the alkoxy analogues and with each other. Product analyses, together with the kinetic data, were used to outline a feasible pathway for the elimination reaction of the compounds under study.

Palladium-catalyzed remote C-H functionalization of 2-aminopyrimidines

Das, Animesh,Jana, Akash,Maji, Biplab

supporting information, p. 4284 - 4287 (2020/04/27)

A straightforward strategy was developed for the arylation and olefination at the C5-position of the N-(alkyl)pyrimidin-2-amine core with readily available aryl halides and alkenes, respectively. This approach was highly regioselective, and the transformation was achieved based on two different (Pd(ii)/Pd(iv)) and (Pd(0)/Pd(ii)) catalytic cycles.

An (Aminopyrimidinato)titanium catalyst for the hydroamination of alkynes and alkenes

Brahms, Christian,Tholen, Patrik,Saak, Wolfgang,Doye, Sven

, p. 7583 - 7592 (2013/12/04)

A new (aminopyrimidinato)titanium complex has been synthesised from inexpensive and easily accessible 2-(tert-butylamino)pyrimidine and [Ti(NMe 2)4] and used as a catalyst for the intermolecular hydroamination of alkynes as well as the cyclization of aminoalkenes. The hydroamination reactions of 1-phenylpropyne and terminal arylalkynes deliver the corresponding anti-Markovnikov addition products with excellent yields and regioselectivities. A new (aminopyrimidinato)titanium complex has been synthesised from inexpensive 2-(tert-butylamino)pyrimidine and [Ti(NMe 2)4] and used as a catalyst for the intermolecular hydroamination of alkynes as well as the cyclization of aminoalkenes. The complex represents the first example of a catalyst for the hydroamination of alkynes that contains an aminoheteroaromatic ancillary ligand.

A divergent synthesis of substituted 2-aminoimidazoles from 2-aminopyrimidines

Ermolat'ev, Denis S.,Van Der Eycken, Erik V.

, p. 6691 - 6697 (2008/12/22)

(Chemical Equation Presented) A new divergent and efficient synthesis of substituted 2-aminoimidazoles 5 and 6 has been developed starting from the readily available 2-aminopyrimidines 1 and α-bromocarbonyl compounds 2, using conventional heating or microwave irradiation. Thus, the cleavage of 1,2,3-substituted imidazo[1,2-a]pyrimidin-1-ium salts 4 with hydrazine or secondary amines led to 1,4,5-trisubstituted 2-aminoimidazoles 5, when the hydrazinolysis of 2-hydroxy-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium salts 3, followed by a novel Dimroth-type rearrangement, resulted in formation of 2-amino-1H-imidazoles 6. The relevant pathway of transformations was identified by characterization of the intermediates.

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