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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789494Generated: October 26, 2026

2-(Methylthio)thiazolo[5,4-b]pyridine → 1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamine

https://huagongshe.com/reaction/1789494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylthio)thiazolo[5,4-b]pyridineHCID 699840—
Reactant1-(4-(Aminomethyl)piperidin-1-yl)ethan-1-oneHCID 12687022—
Product1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamineHCID 2124157593%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 11 parts of 1-acetyl-4-piperidinemethanamine and 9 parts of 2-(methylthio)thiazolo[5,4-b]pyridine was stirred and heated for 20 hours at 140° C. The whole was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 13.5 parts (93%) of 1-acetyl-N-(thiazolo[5,4-b]pyridin-2-yl)-4-piperidinemethanamine as a residue (intermediate 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689330
Source datasetuspto-grants-1987_08
ORD IDord-9e71969e97bc4104b9560ff69314f6e6
Source noteuspto-grants-1987_08