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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75789Generated: October 29, 2026

Potassium Bromide → (S)-2-[(3-{4-[3-(4-Fluoro-phenyl)-ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-4-methyl-pentanoic acid

https://huagongshe.com/reaction/75789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
Reactant(S)-2-[(3-{4-[3-(4-Fluoro-phenyl)-ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-4-methyl-pentanoic acid methyl esterHCID 46181435—
Product(S)-2-[(3-{4-[3-(4-Fluoro-phenyl)-ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-4-methyl-pentanoic acidHCID 4618143658%

Reaction Steps

The title compound was prepared from (S)-2-[(3-{4-[3-(4-Fluoro-phenyl)-ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-4-methyl-pentanoic acid methyl ester using the procedure as set forth in Example 8 and was obtained in 58% yield. Mass (ES+): 455 (M++1); IR (KBr): 3336 (br), 2962, 1724, 1664 (br), 1600, 1543 (br), 1510 (br); 1H NMR (DMSO-d6) δ: 0.87, 0.91 (2×d, 6H), 1.57-1.68 (m, 2H), 1.74-1.82 (m, 1H), 4.41 (m, 1H), 7.12 (t, 2H), 7.46 (m, 2H), 7.59 (d, 2H), 7.61 (s, 1H), 7.82 (d, 2H), 8.80 (s, 1H), 8.97 (s, 1H), 9.17 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835428B2
Source datasetuspto-grants-2014_09
ORD IDord-ffdd51714c574821863888078ff9a846
Source noteuspto-grants-2014_09