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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121679Generated: October 26, 2026

1,1,1-Trimethoxybutane → tert-butyl 4-(6,7-dimethyl-4-phenoxy-2-propyl-1H-imidazo[4,5-c]pyridin-1-yl)butylcarbamate

https://huagongshe.com/reaction/2121679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-TrimethoxybutaneHCID 123512—
ReactantTert-butyl 4-[(3-amino-5,6-dimethyl-2-phenoxypyridin-4-yl)amino]butylcarbamateHCID 12109126—
Producttert-butyl 4-(6,7-dimethyl-4-phenoxy-2-propyl-1H-imidazo[4,5-c]pyridin-1-yl)butylcarbamateHCID 2197382483.1%

Reaction Steps

Using the general method of Example 15 Part E, tert-butyl 4-[(3-amino-5,6-dimethyl-2-phenoxypyridin-4-yl)amino]butylcarbamate (3.41 g, 8.51 mmol) was reacted with trimethyl orthobutyrate (1.50 mL, 9.37 mmol) to provide 3.2 g of crude tert-butyl 4-(6,7-dimethyl4-phenoxy-2-propyl-1H-imidazo[4,5-c]pyridin-1-yl)butylcarbamate as purplish semisolid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696465B2
Source datasetuspto-grants-2004_02
ORD IDord-62c1198847ba4337b3439627852d1703
Source noteuspto-grants-2004_02