4-(Boc-amino)-3-iodopyridine is a chemical compound characterized by its pyridine ring, which is substituted with an iodine atom and a tert-butyloxycarbonyl (Boc) protected amino group. The presence of the iodine atom introduces notable reactivity, making it useful in various synthetic applications, particularly in the field of medicinal chemistry. The Boc group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amine's reactivity. This compound typically appears as a solid and is soluble in organic solvents, which facilitates its use in various chemical reactions. Its structure allows for potential applications in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Additionally, the compound's properties, such as melting point and spectral characteristics, can vary based on purity and specific conditions. Overall, 4-(Boc-amino)-3-iodopyridine is a versatile intermediate in organic synthesis, particularly valued for its functional groups that enable further chemical transformations.

4-(Boc-amino)-3-iodopyridine

211029-67-3: Carbamic acid, N-(3-iodo-4-pyridinyl)-, 1,1-dimethylethyl ester, tert-Butyl (3-iodopyridin-4-yl)carbamate, Carbamicacid,(3-iodo-4-pyridinyl)-,1,1-dimethylethylester(9CI), N-Boc-4-Amino-3-iodopyridine

Carbamic acid, N-(3-iodo-4-pyridinyl)-, 1,1-dimethylethyl ester

(3-Iodo-pyridin-4-yl)-carbamic acid tert-butyl ester

The Buchwald-Hartwig amination is a scalable and versatile method for the synthesis of amines from aryl halides and aminating agents. The catalyzed reaction is an example of a cross-coupling reaction, which proceeds through the formation of an intermediate organometallic species.

The 3-iodopyridine reacts with the tert-butyl bromoacetate to form the corresponding organolithium species, followed by nucleophilic attack by ammonia. This process produces the desired product in high yield.

CAS 211029-67-3: 4-(Boc-amino)-3-iodopyridine

Carbamic acid, N-(3-iodo-4-pyridinyl)-, 1,1-dimethylethyl ester

Ref: IN-DA002L4X

(3-Iodo-pyridin-4-yl)-carbamic acid tert-butyl ester

Ref: 10-F041249

(3-Iodo-pyridin-4-yl)carbamic acid tert-butyl ester

Ref: 3D-FI50903

(3-Iodo-pyridin-4-yl)-carbamic acid tert-butyl ester

Ref: 54-OR913048