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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396726Generated: October 26, 2026

3-Methyl-5-isoxazolecarboxylic acid → Methyl (R) 3-(1-boc-1,2,3,4-Tetrahydro-quinolin-6-yl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionate

https://huagongshe.com/reaction/396726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-5-isoxazolecarboxylic acidHCID 76947—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 69563649HCID 69563649—
SolventDimethylformamideHCID 6228—
ProductMethyl (R) 3-(1-boc-1,2,3,4-Tetrahydro-quinolin-6-yl)-3-[(5-methyl-isoxazole-3-carbonyl)-amino]-propionateHCID 86759118—

Reaction Steps

A solution of 5-methyl-isoxazole-3-carboxylic acid (65 mg) in dimethylformamide (30 ml) was treated successively with O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (190 mg), diisopropylethylamine (1 ml) and methyl (R) 3-amino-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionate (200 mg, Reference Example 14). After standing at room temperature overnight the mixture was evaporated to low bulk and the residue partitioned between ethyl acetate and dilute hydrochloric acid. The layers were separated and the organic layer was washed with sodium carbonate solution, dried, and evaporated. The residue was purified by flash chromatography to give the title compound as an orange gum, 310 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608084B1
Source datasetuspto-grants-2003_08
ORD IDord-e93d24a103e14d3699559b4987aab17e
Source noteuspto-grants-2003_08