Glycine → 3061-96-9

HRID 2398321Notes

Reaction equation

HRID 2398321 reaction equation
[NH2:1][CH:2]([C:7]([OH:9])=O)[CH2:3][CH2:4][S:5][CH3:6].NCC(O)=O.[NH2:15][C@H:16]([C:21]([OH:23])=[O:22])[CH2:17]CSC.N[C@H](C(O)=O)C>O>[NH2:1][C@H:2]([C:7]([NH:15][C@H:16]([C:21]([OH:23])=[O:22])[CH3:17])=[O:9])[CH2:3][CH2:4][S:5][CH3:6]

Participants

6

Reactant 4

HCID 750GlycineHCID 876(+-)-MethionineHCID 5950L-Alanine2×HCID 6137L-Methionine2×

Product 1

HCID 70095813061-96-9

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The title compound was prepared according to the procedures of Example 1A and B above by replacing DL-methionine and glycine respectively with L-methionine and L-alanine (Aldrich Chemical Co., Beil. 4,381). The title compound had a melting point of 141° to 143° C (d). The compound was found to be water soluble. The product thus obtained was subjected to amino acid analysis and found to contain 49.40 mole percent alanine and 50.60 mole percent methionine.

Workup

  1. customThe title compound was prepared
  2. customThe product thus obtained

Sources & evidence

ORD record
ord-18b36f766312433f8a3dd2c3d830dded
Source dataset
uspto-grants-1977_05
Patent number
US04024286

Reaction notes

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