Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72126Generated: October 27, 2026

Hydrochloric Acid → 2-Adamantyl 3-((tert-butoxycarbonylamino)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/72126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-adamantyl ChloroformateHCID 10878537—
Reactanttert-butyl N-(azetidin-3-ylmethyl)carbamateHCID 15346872—
Product2-Adamantyl 3-((tert-butoxycarbonylamino)methyl)azetidine-1-carboxylateHCID 4447336623%

Reaction Steps

A vial was charged with tert-butyl azetidin-3-ylmethylcarbamate (25 mg, 0.12 mmol), i-Pr2NEt (31 μL, 0.17 mmol) and a flea stir bar. A solution of 2-adamantyl chloroformate in CH2Cl2 (1.5 mL, 17 mg mL−1, 0.12 mmol) was added. The mixture was stirred overnight at rt. A 10-mL ChemElut cartridge (Varian Inc. catalog number 12198007) was wetted with 5% aq HCl (5 mL) and allowed to stand for 5 min. The reaction mixture was applied to the cartridge and eluted with ether (20 mL). The eluate was evaporated to dryness and the residue was purified by preparative HPLC to afford the title compound (10 mg, 23%). 1H NMR (CDCl3) δ 1.42 (s, 9H), 1.5-2.0 (14H), 2.76 (m, 1H), 3.35 (m, 2H), 3.67 (m, 2H), 4.03 (m, 2H), 4.68 (m, 1H), 4.78 (s, 1H); LC-MS Method 1 tR=2.08 min, m/z=387, 365, 309.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828985B2
Source datasetuspto-grants-2014_09
ORD IDord-2d93cf5715574d9f865ec399ec289624
Source noteuspto-grants-2014_09