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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808896Generated: October 30, 2026

3-(2-Methoxyphenyl)-5-methyl-1,2-oxazole-4-carboxylic acid → Methyl 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzoate

https://huagongshe.com/reaction/1808896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Methoxyphenyl)-5-methyl-1,2-oxazole-4-carboxylic acidHCID 6484100—
ReactantMethyl 2-amino-5-chloro-4-(piperazin-1-yl)benzoateHCID 66691661—
ProductMethyl 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzoateHCID 66691522—

Reaction Steps

3-(2-Methoxyphenyl)-5-methylisoxazole-4-carboxylic acid and methyl 2-amino-5-chloro-4-(piperazin-1-yl)benzoate (TFA salt) were coupled under the conditions described in Preparation M to give methyl 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzoate. 1H-NMR (CDCl3, 400 MHz): δ 7.82 (1H, s), 7.60-7.47 (2H, m), 7.13-6.97 (2H, m), 6.01 (1H, s), 3.85 (3H, s), 3.84 (2H, s), 3.80 (3H, s), 3.25 (2H, s), 2.99 (2H, s), 2.58 (3H, s), 2.42 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362004B2
Source datasetuspto-grants-2013_01
ORD IDord-0ea6e755639e4e1f91f33787008c0f79
Source noteuspto-grants-2013_01