Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336532Generated: October 29, 2026

Diisopropylethylamine → tert-Butyl 2-[(3-(methylcarbamoyl)isoxazol-5-ylmethoxycarbonylamino)methyl]-6-azaspiro[3.4]octane-6-carboxylate

https://huagongshe.com/reaction/336532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Methylcarbamoylisoxazol-5-ylmethyl 4-nitrophenyl carbonateHCID 66660764—
Reactanttert-Butyl 2-(aminomethyl)-6-azaspiro[3.4]octane-6-carboxylateHCID 68001449—
Producttert-Butyl 2-[(3-(methylcarbamoyl)isoxazol-5-ylmethoxycarbonylamino)methyl]-6-azaspiro[3.4]octane-6-carboxylateHCID 68001372—

Reaction Steps

The process is performed according to the procedure described in Example 1, step 1.1. Starting with 0.22 g (0.92 mmol) of tert-butyl 2-aminomethyl-6-azaspiro[3.4]octane-6-carboxylate (isomer 2a), described in Example 8 (step 8.2.), 0.294 g (0.92 mmol) of 3-(methylcarbamoyl)isoxazol-5-ylmethyl 4-nitrophenyl carbonate, obtained in step 4.1., 0.236 g (1.83 mmol) of N,N-diisopropylethylamine and 0.011 g (0.09 mmol) of N,N-dimethylaminopyridine, and after purification by chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 0.310 g of pure product is thus obtained in the form of an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889702B2
Source datasetuspto-grants-2014_11
ORD IDord-31fe5462f74d4b289c2355569a94fee1
Source noteuspto-grants-2014_11