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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914464Generated: October 26, 2026

4-Methyl-1-pentanol → 2-[(4-{2-[(5-Ethylpyrimidin-2-yl)(4-methylpentyl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid hydrogen bromide

https://huagongshe.com/reaction/914464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-1-pentanolHCID 12296—
Reactant1-Iodo-4-methylpentaneHCID 527581—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
Reactant2-[(4-{2-[(5-Ethylpyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl esterHCID 59758871—
SolventDiethyl EtherHCID 3283—
Product2-[(4-{2-[(5-Ethylpyrimidin-2-yl)(4-methylpentyl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid hydrogen bromideHCID 67400871—

Reaction Steps

A compound obtained using 1-iodo-4-methylpentane, which is synthesized using 2-[(4-{2-[(5-ethylpyrimidin-2-yl)amino]ethyl}-1,3-thiazol-2-yl)thio]-2-methylpropionic acid tert-butyl ester synthesized in Example 265-1 and 4-methylpentanol as starting materials and in reference to non-patent reference [Tetrahedron, 38, 11461 (1998)], and by an operation similar to that of Example 326, was dissolved in diethyl ether, and reacted with 30% hydrobromic acid-acetic acid to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-0c832d8449ba48bfa70bc97c3d7c71aa
Source noteuspto-grants-2011_09