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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249Generated: October 28, 2026

Methyl 2-t-butoxycarbonylamino-4-[4-[4-(4-pyridyl)-piperazin-1-yl]phenoxy]butyrat → Methyl 2-amino-4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]butyrate

https://huagongshe.com/reaction/2249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-t-butoxycarbonylamino-4-[4-[4-(4-pyridyl)-piperazin-1-yl]phenoxy]butyratHCID 18918622—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 2-amino-4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]butyrateHCID 1891821474.1%

Reaction Steps

The compound of Example 140 (0.96 g) in TFA (10 ml) was kept at room temperature for 2 hours. The solution was evaporated and the residue dissolved in water (15 ml) and the solution basified with sodium carbonate. The mixture was extracted three times with dichloromethane. Evaporation of the combined extracts gave the title compound (0.56 g); m.p. 125°-127° C.; NMR(d6DMSO) δ 8.2(2H,d), 6.92(6H,m), 4.0(2H,m), 3.64(3H,s), 3.46(4H,t), 3.15(4H,t), 2.04(2H,m), 1.84(1H, m); m/e 371(M+H)+. Calculated for C20H26N4 O3. 0.75 H2O: C, 62.5; H, 7.17; N, 14.6. Found: C, 62.8; H, 6.8; N, 14.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728701
Source datasetuspto-grants-1998_03
ORD IDord-bc4c5bfd0a2540ebba7d4dbbdd3411b3
Source noteuspto-grants-1998_03