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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713257Generated: November 3, 2026

(S)-(+)-1-Aminopropan-2-ol → HCID 21089034, compound

https://huagongshe.com/reaction/1713257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-1-Aminopropan-2-olHCID 7311736—
Reactant(+/-) 3-[5-chloro-4-((2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamideHCID 21089004—
ProductHCID 21089034HCID 2108903453%

Reaction Steps

The title compound was prepared by a procedure similar to the one described for (±) 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-2-methyl-6-oxopyrimidin-1(6H)-yl]-N-(2-hydroxyethyl)-4-methylbenzamide using (S)-(+)-1-amino-2-propanol (0.98 mL, 12.45 mmol) as the amine. After reverse phase HPLC purification, the organic extracts were concentrated under reduced pressure and dried in vacuo to afford the desired product (2.13 g, 53%) as white solid. 1H-NMR (CD3OD, 400 MHz) δ 7.93 (dd, 1H, J=1.6 Hz), 7.69 (d, 1H, J=1.6 Hz), 7.62 (m, 1H), 7.56 (d, 1H, J=8 Hz), 7.01 (m, 2H), 5.59 (q, 2H, J=12.4 Hz), 3.94 (m, 1H), 3.39 (m, 2H), 2.18 (s, 3H), 2.13 (s, 3H), 1.9 (d, 3H, J=6.4 Hz); ES-HRMS m/z 478.1308 (M+H C23H23ClF2N3O4 requires 478.1340). Both (+) and (−) atropomers will be resolved and characterized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795271B2
Source datasetuspto-grants-2010_09
ORD IDord-c937ea14775d4406902c1c7e02e3f50f
Source noteuspto-grants-2010_09