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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370953Generated: November 2, 2026

Ethyl N-methylaminoacetate hydrochloride → N-[(4-{4-[(benzyl{2-methyl-3-[(methylsulfonyl)amino]phenyl}amino)methyl]phenoxy}phenoxy)acetyl]-N-methylglycine

https://huagongshe.com/reaction/1370953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl N-methylaminoacetate hydrochlorideHCID 171173—
Reactant(4-(4-((Benzyl(2-methyl-3-((methylsulfonyl)amino)phenyl)amino)methyl)phenoxy)phenoxy)acetic acidHCID 11410199—
ProductN-[(4-{4-[(benzyl{2-methyl-3-[(methylsulfonyl)amino]phenyl}amino)methyl]phenoxy}phenoxy)acetyl]-N-methylglycineHCID 18512118—

Reaction Steps

The product from Example 95C and N-methylglycine ethyl ester hydrochloride were processed as described in Example 251A and B to provide the titled compound. 1H NMR (500 MHz, DMSO-d6) δ12.40-13.15 (br.s, 1 H), 8.94 (s, 1 H), 7.23 (m, 7 H), 7.03 (t, 1 H), 6.93 (m, 6 H), 6.82 (dd, 2 H), 4.84 (s, 1 H), 4.69 (s, 1 H), 4.17 (s, 1 H), 4.05 (s, 2 H), 4.00 (m, 3 H), 3.04 (s, 2 H), 2.91 (s, 3 H), 2.85 (s, 1 H), 2.39 (s, 3 H); MS (ESI+) m/z 618 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583180B2
Source datasetuspto-grants-2003_06
ORD IDord-947b5656b10b4b4ab441a9ec0a2f1f15
Source noteuspto-grants-2003_06