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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425910Generated: November 1, 2026

Sodium Azide → Tert-butyl n-(2-azido-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate

https://huagongshe.com/reaction/1425910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantN,N'-di-Boc-2-methanesulfonyloxy-1,3-diaminopropaneHCID 14839452—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductTert-butyl n-(2-azido-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamateHCID 1518600167%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl N-(3-{[(tert-butoxy)carbonyl]amino}-2-(methanesulfonyloxy)propyl)carbamate XXVII (2.31 g, 6.6 mmol) in DMF was added NaN3. The mixture was heated overnight at 60° C., diluted with DCM and washed with 10% Na2S2O3 (5×), 5% NaHCO3, brine and dried over MgSO4. The solvent was evaporated under vacuum to give crude product (1.75 g). The product was purified on a silica gel column (1:10 EtOAc:hexane) to give the pure tert-butyl N-(2-azido-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate XXVIII as white crystals (1.33 g, 4.2 mmol, 67% yield). 1H NMR (CDCl3) δ ppm 1.47 (s, 18H), 3.07-3.26 (m, 2H), 3.27-3.53 (m, 2H), 3.59-3.75 (m, 1H), 5.06 (brs, 2H); ESIMS found for C13H25N5O4 m/z 316 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933018B2
Source datasetuspto-grants-2015_01
ORD IDord-fd258496416d45839c96587cb86fe1c2
Source noteuspto-grants-2015_01