Glycine → tert-butyl N-({2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]phenyl}carbonyl)glycinate

HRID 1502214Notes

Reaction equation

HRID 1502214 reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]([C:13]2[N:21]3[C:16]([CH:17]=[CH:18][CH:19]=[CH:20]3)=[C:15]([Br:22])[C:14]=2[CH3:23])=[O:12])=[CH:7][C:3]=1[C:4](O)=[O:5].[NH2:24][CH2:25][C:26]([OH:28])=[O:27]>>[NH2:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]([C:13]2[N:21]3[C:16]([CH:17]=[CH:18][CH:19]=[CH:20]3)=[C:15]([Br:22])[C:14]=2[CH3:23])=[O:12])=[CH:7][C:3]=1[C:4]([NH:24][CH2:25][C:26]([O:28][C:3]([CH3:7])([CH3:4])[CH3:2])=[O:27])=[O:5]

Participants

3

Reactant 2

HCID 750GlycineHCID 666531732-Amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoic acid

Product 1

HCID 117776412tert-butyl N-({2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]phenyl}carbonyl)glycinate

Procedure

Obtained according to the process described in Step 1.5, using 2-amino-5-[(1-bromo-2-methylindolizin-3-yl)carbonyl]benzoic acid and the tert-butyl ester of glycine, in the form of a yellow powder (74%).

Workup

  1. customObtained

Sources & evidence

ORD record
ord-7170ec92e3c14f82b5ec4d3d54d62861
Source dataset
uspto-grants-2015_12
Patent number
US09206177B2

Reaction notes

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