N-((1,1-dimethylethoxy)carbonyl)-beta-alanine → HCID 28238191, compound

HRID 1621110Notes

Reaction equation

HRID 1621110 reaction equation
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12])=[O:7])([CH3:4])([CH3:3])[CH3:2].Br[CH2:15][C:16]([C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=1)=[O:17]>>[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][C:11]([O:13][CH2:15][C:16]([C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([O:24][CH3:25])[CH:19]=1)=[O:17])=[O:12])=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 76809N-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 101294Bromomethyl 3-methoxyphenyl ketone

Product 1

HCID 28238191HCID 28238191, compound

Procedure

The product was obtained starting from 3-(tert-butoxycarbonylamino)propanoic acid (400 mg, 2.11 mmol) and 2-bromo-1-(3-methoxyphenyl)ethanone (484 mg, 2.11 mmol) according to the method described in example 7, step 1 as yellow oil (759 mg, 2.11 mmol, 100%). MS: M=238.2 (M-Boc+H)+

Workup

  1. customThe product was obtained

Sources & evidence

ORD record
ord-3597919e0aae4c2c8a2cbe34577d5c78
Source dataset
uspto-grants-2014_07
Patent number
US08772510B2

Reaction notes

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