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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231898Generated: October 31, 2026

Methyl trans-2-(3-bromo-2-oxopropyl)-3-methoxypiperidine-1-carboxylate → Methyl trans-2-[3-(6-Trifluoromethylquinazolin-4(3H)-on-3-yl)-2-oxopropyl]-3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/231898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl trans-2-(3-bromo-2-oxopropyl)-3-methoxypiperidine-1-carboxylateHCID 86741990—
Reactant6-(Trifluoromethyl)quinazolin-4(1H)-oneHCID 135745155—
ProductMethyl trans-2-[3-(6-Trifluoromethylquinazolin-4(3H)-on-3-yl)-2-oxopropyl]-3-methoxypiperidine-1-carboxylateHCID 8674232324%

Reaction Steps

By the method of Example 4, 6-trifluoromethyl- quinazolin-4-(3H)-one and methyl trans-2-(3-bromo-2-oxoproyl)3-methoxypiperidine-1-carboxylate were converted into the title compound in 24% yield; m.p. 137°-140° C. 1H-NMR(CDCl3) 1.4-1.9 (m, 4H), 2.9 (d, 2H), 3.3 (s, 3H), 3.5-3.9 (m,4H), 3.7 (s, 3H), 5.2 (s, 2H), 7.7-8.7 (m,4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849518
Source datasetuspto-grants-1989_07
ORD IDord-16e693ac97084b61b547a1f93783b08a
Source noteuspto-grants-1989_07