tert-butyl N-(azetidin-3-ylmethyl)carbamate → 3-(N-Boc)-(2-aminoethyl)azetidine

HRID 874

Reaction equation

HRID 874 reaction equation
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH:11]1[CH2:14][N:13](C(C2C=CC=CC=2)C2C=CC=CC=2)[CH2:12]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(OC(NCC1CNC1)=O)(C)(C)C>>[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH:11]1[CH2:12][NH:13][CH2:14]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 15346872tert-butyl N-(azetidin-3-ylmethyl)carbamateHCID 541817273-(N-tert-butyloxycarbonylaminoethyl)-1-benzhydryl azetidine

Product 1

HCID 378184313-(N-Boc)-(2-aminoethyl)azetidine

Procedure

The title compound was prepared from 3-(N-tert-butyloxycarbonylaminoethyl)-1-benzhydryl azetidine according the procedure for 3-(N-tert-butyloxycarbonylaminomethyl) azetidine, in a yield of 1.2 g (70%).

Sources & evidence

ORD record
ord-b116e8105ba1433db653190ba3814a43
Source dataset
uspto-grants-1998_03
Patent number
US05723444

Linked notes

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