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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905504Generated: October 31, 2026

3-Amino-1,2-propanediol → 5-Oxazolemethanol, 4,5-dihydro-2-(4-((7-(3-methyl-5-isoxazolyl)heptyl)oxy)phenyl)-

https://huagongshe.com/reaction/1905504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-1,2-propanediolHCID 73561—
Reactant5-Methyl-3-isoxazolepropionic acidHCID 133360—
Reactant5-[7-(4-Cyanophenoxy)heptyl]-3-methylisoxazoleHCID 5271208—
Product5-Oxazolemethanol, 4,5-dihydro-2-(4-((7-(3-methyl-5-isoxazolyl)heptyl)oxy)phenyl)-HCID 527215960%

Reaction Steps

5-{7-[4-(4,5-Dihydro-5-hydroxymethyl-2-oxazolyl)phenoxy]heptyl}-3-methylisoxazole [IX; R=CH3, R1, R2, R3, R4 and R5 =H, R6 =CH2OH, Y=(CH2)7, oxazole at 4-position] was prepared from the ethyl imino-ester hydrochloride of 5-[7-(4-cyanophenoxy)heptyl]-3-methylisoxazole and 3-amino-1,2-propanediol according to the procedure of Example 1, part (c), and was obtained in about 60% yield in the form of a colorless solid, m.p. 75°-76° C., when recrystallized first from isopropyl acetate and then from acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843087
Source datasetuspto-grants-1989_06
ORD IDord-8324eca4c3444487b42aa70748b30d7a
Source noteuspto-grants-1989_06