Acetic Acid → N-{4-[2-(4-Amino-2-imino-2,3-dihydropyrido[2,3-d]pyrimidin-6-yl)ethyl]benzoyl}glutamic acid

HRID 1494618Notes

Reaction equation

HRID 1494618 reaction equation
[NH2:1][C:2]1[N:3]=[C:4]([NH2:36])[C:5]2[CH:11]=[C:10]([CH2:12][CH2:13][C:14]3[CH:35]=[CH:34][C:17]([C:18]([NH:20][C@H:21]([C:29]([O:31]CC)=[O:30])[CH2:22][CH2:23][C:24]([O:26]CC)=[O:25])=[O:19])=[CH:16][CH:15]=3)[CH:9]=[N:8][C:6]=2[N:7]=1.[OH-].[Na+].C(O)(=O)C>CO>[NH2:1][C:2]1[N:3]=[C:4]([NH2:36])[C:5]2[CH:11]=[C:10]([CH2:12][CH2:13][C:14]3[CH:15]=[CH:16][C:17]([C:18]([NH:20][C@H:21]([C:29]([OH:31])=[O:30])[CH2:22][CH2:23][C:24]([OH:26])=[O:25])=[O:19])=[CH:34][CH:35]=3)[CH:9]=[N:8][C:6]=2[N:7]=1

Participants

5

Procedure

A solution of 0.38 g of diethyl N-(4-[2-(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)ethyl]benzoyl)-L-glutamate in 50 mL of methanol containing 4.6 mL of 0.5N aqueous sodium hydroxide was stirred at room temperature for 72 hours. Acetic acid (5 mL) was added, and the resulting white precipitate collected by filtration. The filter cake was washed well with water, methanol, and ether and was dried under reduced pressure to yield 0.15 g (44%) of the title compound, which can be alternatively named as 5,10-dideazaaminopterin; mp>250° C.; NMR (TFA-d1) delta 2.2-2.7(m, 2H), 2.28; 2.7-2.95(m, 2H), 5.0-5.2(m, 1H), 7.35 and 7.85(AB q, 4H, J=9 Hz), 8.7(s, 1H), 9.1(s, 1H).

Workup

  1. filtrationthe resulting white precipitate collected by filtration
  2. washThe filter cake was washed well with water, methanol, and ether
  3. customwas dried under reduced pressure

Sources & evidence

ORD record
ord-8117344964064687833ed0f0b525baf1
Source dataset
uspto-grants-1991_06
Patent number
US05026851

Reaction notes

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