Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660788Generated: November 1, 2026

Ethyl 4-amino-2-methylbenzoate → 4-{[4-(5-chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-2-methyl-benzoic acid ethyl ester

https://huagongshe.com/reaction/1660788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-amino-2-methylbenzoateHCID 24721080—
Reactant4-{[4-(5-Chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-2-methyl-benzoic acidHCID 24762473—
Product4-{[4-(5-chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-2-methyl-benzoic acid ethyl esterHCID 66788782—

Reaction Steps

4-{[4-(5-Chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-2-methyl-benzoic acid, MS (ISP): m/e=515.0 (M−H), was prepared as described in example 1, steps 1 to 6. Step 5 was performed using 4-amino-2-methyl-benzoic acid ethyl ester and yielded 4-{[4-(5-chloro-2-methoxy-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl]-amino}-2-methyl-benzoic acid ethyl ester, which was hydrolyzed in step 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030308B2
Source datasetuspto-grants-2011_10
ORD IDord-643829f7e0e7432995bac517701865a0
Source noteuspto-grants-2011_10