Methylamine → 3-(Benzyloxycarbonylamino)-1-propoxyamine

HRID 48878Notes

Reaction equation

HRID 48878 reaction equation
[CH2:1]([O:8][C:9]([NH:11][C:12]1[CH:13]2C(=O)NC(=O)[C:14]2([O:23]CCC)C=CC=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O1CCCC1.C[NH2:33]>C(O)C>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][CH2:14][O:23][NH2:33])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 6329MethylamineHCID 8028TetrahydrofuranHCID 1317226343-(Benzyloxycarbonylamino)-1-propoxylphthalimide

Product 1

HCID 117757963-(Benzyloxycarbonylamino)-1-propoxyamineYield 97%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a solution of N-[3-(benzyloxycarbonylamino)-1-propoxylphthalimide (1.42 g, 4.0 mmol), as prepared in the preceding step, in ethanol (20 mL) and tetrahydrofuran (20 mL) was added 40% methylamine (2 mL, 25 mmol). The solution was stirred at room temperature for 1 h. The solvent was evaporated and the residue passed through silica gel (3:1 ethyl acetate:hexane to ethyl acetate) to give the title compound as a white solid (870 mg, 97%). 1H-NMR (300 MHz, CDCl3) δ7.36 (m, 5H), 5.38 (br s, 2H), 5.09 (s, 2H), 5.08 (br s, 1H), 3.73 (t, J=5.9 Hz, 2H), 3.29 (q, J=6.2 Hz, 2H), 1.79 (pentet, J=6.2 Hz, 2H).

Workup

  1. customThe solvent was evaporated

Sources & evidence

ORD record
ord-5738fd1b045e4fd6befaf6c1d7d5c5d6
Source dataset
uspto-grants-2004_03
Patent number
US06706021B2

Reaction notes

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