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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065547Generated: October 31, 2026

1-(Bromomethyl)-2-chloro-4-fluorobenzene → 6-[3 (R)-Amino-piperidin-1-yl]-1-(2-chloro-4-fluoro-benzyl)-3-methyl-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/2065547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-2-chloro-4-fluorobenzeneHCID 2725062—
ReactantTrelagliptin Impurity 47HCID 11464036—
Product6-[3 (R)-Amino-piperidin-1-yl]-1-(2-chloro-4-fluoro-benzyl)-3-methyl-1H-pyrimidine-2,4-dioneHCID 11314596—

Reaction Steps

The title compound was prepared from compound 1 using the same procedures as described the preparation of compound 10, except that 2-chloro-4-fluoro-benzyl bromide was used in the place of 2-bromo-5-fluoro-benzyl bromide. 1H-NMR (400 MHz, CDCl3-CD3OD 10:1) δ 7.15 (dd, J=8.211, 2.400 Hz, 1 H), 6.95-7.06 (m, 2 H), 5.40 (s, 1 H), 5.09-5.18 (ABq, J=37.7, 15.9 Hz, 2H), 3.33-3.39 (m, 1 H), 3.30 (s, 3 H), 3.23-3.29 (m, 1H), 2.98 (bd, J=12.9 Hz, 1 H), 2.79 (t, J=10.4 Hz, 1 H), 2.55-2.66 (t, J=11.2 Hz, 1 H), 2.13 (m, 1 H), 1.78-1.88 (m, 1 H), 1.55-1.65 (m, 2 H). MS (ES) [m+H] calc'd for C17H21ClFN4O2, 367.1. found 367.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288539B2
Source datasetuspto-grants-2012_10
ORD IDord-20be3bef3c8b4b0b856032be7db1557d
Source noteuspto-grants-2012_10