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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648299Generated: October 27, 2026

Methylamine → t-Butyl (1,2,5,6-tetrahydro-2-oxo-4H-imidazo(4,5,1-ij)quinolin-5-yl)carbamate

https://huagongshe.com/reaction/1648299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPhosgeneHCID 6371—
Reactantt-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamateHCID 19108500—
SolventTetrahydrofuranHCID 8028—
Productt-Butyl (1,2,5,6-tetrahydro-2-oxo-4H-imidazo(4,5,1-ij)quinolin-5-yl)carbamateHCID 15937764—

Reaction Steps

t-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate (2.70 g) was dissolved in THF (100 mL) and stirred while a solution of phosgene in THF (20.7 mL of 0.40 M, 0.093 mol) was added. After 5 minutes, methylamine (2.08 g, 0.020 mol) was added and the solution stirred for an additional 10 minutes. The THF was removed under reduced pressure and the material was partitioned between chloroform (250 mL) and water (20 nil,). The chloroform was washed with 4N sodium hydroxide (5 mL) and evaporated. The crude material was combined with that of an earlier reaction (0.002 mol scale) and purified by chromatography on silica gel in 1% methanol: chloroform to give 2.28 g of product. Crystallization from methanol:ether (1:1) gave 1.60 g (54%) white solid, mp 235°-36° C. Anal. Calc'd for C15H19N3O3 : C, 62.26; H, 6.62; N, 14.52. Found: C, 61.65; H, 6.94; N, 14.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436240
Source datasetuspto-grants-1995_07
ORD IDord-68fa5fcc34434be0ac0d60429fda00ba
Source noteuspto-grants-1995_07