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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073939Generated: October 29, 2026

Allyl trans-2-(3-bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylate → HCID 86743238, compound

https://huagongshe.com/reaction/2073939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl trans-2-(3-bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylateHCID 86741991—
ReactantHCID 135745158HCID 135745158—
ProductHCID 86743238HCID 86743238—

Reaction Steps

In the manner of Example 4, 1.09 g (0.003 mol) of 7-iodo-6-methylthioquinazolin-4(3H)-one formic acid salt and 1.0 g (0.003 mol) of allyl trans-2-(3-bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylate were converted into the title compound: yield 0.53 g (31%); mass spectrum m/e 571 (molecular ion), 539 (-32, --CH3OH), 221 (parent peak). 1H--NMR(CDCl3) 1.4-2.1 ppm (multiplet, 4H, OCHCH2CH2CH2N), 2.6 (singlet, 3H, SCH3), 2.8-3.4 (multiplet, 4H, NCH2, COCH2CH), 3.4 (singlet, 3H, OCH3), 4.0 (broad singlet, 1H, CHNCO), 4.6 (doublet, 2H, CH2CH=CH2), 5.0 (singlet, 2H, NCH2CO), 5.0-5.5 (multiplet, 2H, CH=CH2), 5.6-6.1 (octet, 1H, CH2 = CH), 7.7 (singlet, 1H, aromatic H), 7.8 (singlet, 1H, N=CH--N), 8.2 (singlet, 1H, aromatic H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920224
Source datasetuspto-grants-1990_04
ORD IDord-a47fe1217da9412cb8c163e328d9116d
Source noteuspto-grants-1990_04