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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587152Generated: October 28, 2026

(2R)-2-(Methoxymethyl)pyrrolidine → (R)-3-[(4-(2-(Methoxymethyl)pyrrolidin-1-yl)-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide

https://huagongshe.com/reaction/587152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-2-(Methoxymethyl)pyrrolidineHCID 671216—
Reactant3-[(4-(Piperidin-1-yl)-1,3,5-triazin-2-yl)amino]benzenemethane sulfonamideHCID 60197101—
Reactant3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—
Product(R)-3-[(4-(2-(Methoxymethyl)pyrrolidin-1-yl)-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 60197304—

Reaction Steps

B17 was prepared following the procedure reported for B1 using A1 and (R)-2-(methoxymethyl)pyrrolidine. 1H NMR (400 MHz, DMSO, 300K) δ 1.85-2.01 (m, 4H), 3.25 (s, 3H), 3.31-3.63 (m, 4H), 4.18-4.29 (m, 3H), 6.81 (s, 2H), 6.98 (t, J=8.4 Hz, 1H), 7.25 (dt, J=4.7 Hz, J=7.8 Hz, 1H), 7.65-7.87 (m, 2H), 8.20 (s, 1H), 9.63 (s, 1H). MS (ES) C16H22N6O3S requires: 378. found: 379 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226929B2
Source datasetuspto-grants-2016_01
ORD IDord-657b3cd4774b459783d76b56bd203389
Source noteuspto-grants-2016_01