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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649843Generated: November 1, 2026

Triethylamine → 2-Amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole

https://huagongshe.com/reaction/1649843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiazolamine, 4-(chloromethyl)-, hydrochloride (1:1)HCID 73228—
Reactant4-BenzhydryloxypiperidineHCID 3017584—
SolventDimethylformamideHCID 6228—
Product2-Amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazoleHCID 1985493770.4%

Reaction Steps

A stirred mixture of 2-amino-4-chloromethylthiazole hydrochloride (0.7 g), 4-(diphenylmethoxy)piperidine (0.78 g) and triethylamine (1.82 ml) in N,N-dimethylformamide (7.8 ml) was heated at 40° C. to 45° C. for 5 hours. After cooling to ambient temperature, the reaction mixture was filtered. The filtrate was poured into water (50 ml) and extracted with ethyl acetate (80 ml×2). The extract was washed with a saturated aqueous solution of sodium chloride (30 ml) and dried over magnesium sulfate. The solvent was distilled off and the residue was subjected to column chromatography on silica gel (30 g) and eluted with a mixture of chloroform and methanol (10:1 V/V). The fractions containing the object compound were combined and concentrated under reduced pressure to give 2-amino-4-[4-(diphenylmethoxy)piperidinomethyl]thiazole (0.78 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921887
Source datasetuspto-grants-1990_05
ORD IDord-a215d011ffc14004bdad469d90986a1b
Source noteuspto-grants-1990_05