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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291900Generated: October 29, 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/1291900

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 211 (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 numberUS05753659
Source datasetuspto-grants-1998_05
ORD IDord-e66f592dba904e029addc982b93c77b9
Source noteuspto-grants-1998_05