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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75817Generated: October 27, 2026

Dicyclohexylcarbodiimide → 2-[(3-{4-[3-(2-Fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl ester

https://huagongshe.com/reaction/75817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethyl valinate hydrochlorideHCID 111190—
Reactant3-(4-(3-(2-Fluorophenyl)ureido)phenyl)isoxazole-5-carboxylic acidHCID 67353981—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[(3-{4-[3-(2-Fluoro-phenyl)ureido]-phenyl}-isoxazole-5-carbonyl)-amino]-3-methyl-butyric acid methyl esterHCID 6735242282.6%

Reaction Steps

3-(4-(3-(2-fluorophenyl)ureido)phenyl)isoxazole-5-carboxylic acid (1 g) was dissolved in DMF (20 ml). N,N′-Dicyclohexyl carbodiimide (906 mg) and 1-Hydroxy benzotriazole (396 mg) were added and the reaction mixture was stirred at RT for 15 minutes. L-Valine methyl ester hydrochloride (640 mg) was dissolved in DMF (5 ml), neutralized with TEA (0.53 ml) and added into the above reaction mixture, which was then stirred at RT for 16 h. DMF was removed under reduced pressure to get a pale brown solid which was taken in water and extracted with EtOAc. Organic layer was dried over Na2SO4 and concentrated to get a pale yellow solid which was purified by silica gel column chromatography in 2:8 EtOAc:CHCl3 to get off white solid which was crystallized from DCM/Pet ether to yield 1.1 gm (82%) white solid. 1HNMR (DMSO-d6, 300 MHz): δ 9.33 (s, 1H), 9.18 (d, 1H), 8.62 (s, 1H), 8.13 (m, 1H), 7.85 (d, 2H), 7.67 (s, 1H), 7.59 (d, 2H), 7.24 (m, 1H), 7.16 (m, 1H), 7.02 (m, 1H), 4.29 (m, 2H), 3.66 (s, 3H), 2.2 (m, 1H), 0.95 (d, 6H); MS (ES+): m/z 455 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835428B2
Source datasetuspto-grants-2014_09
ORD IDord-6da1778bdb584939909a0d7ebb3cf1c6
Source noteuspto-grants-2014_09