Pyridine → HCID 20162879, compound

HRID 2118556Notes

Reaction equation

HRID 2118556 reaction equation
[NH2:1][C:2]1([NH:7][C:8](=[O:28])[CH:9]([C:15]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=2)=[O:16])[C:10]2[CH:14]=[CH:13][S:12][CH:11]=2)[CH2:5][NH:4][C:3]1=[O:6].N1C=CC=CC=1.[C:35](OC=O)(=[O:37])C>ClCCl>[CH:35]([NH:1][C:2]1([NH:7][C:8](=[O:28])[CH:9]([C:15]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=2)=[O:16])[C:10]2[CH:14]=[CH:13][S:12][CH:11]=2)[CH2:5][NH:4][C:3]1=[O:6])=[O:37]

Participants

5

Reactant 3

HCID 1049PyridineHCID 75269Acetic-formic anhydrideHCID 20162869HCID 20162869, compound

Product 1

HCID 20162879HCID 20162879, compoundYield 97.3%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

The amine (42) (490 mg) in dry dichloromethane was cooled to 0° C. and treated with pyridine (211 mg) followed by formic-acetic anhydride (117 mg). The mixture was stirred at 0° C. for 5 minutes then allowed to warm to room temperature. After 1/2 hour the solvent was evaporated and the residue dried in vacuo. The solid was triturated with dry ether, filtered off, and washed with more ether before drying in vacuo to give the product (43) (510 mg) as a white solid.

Workup

  1. temperatureto warm to room temperature
  2. customAfter 1/2 hour the solvent was evaporated
  3. customthe residue dried in vacuo
  4. customThe solid was triturated with dry ether
  5. filtrationfiltered off
  6. washwashed with more ether
  7. custombefore drying in vacuo

Sources & evidence

ORD record
ord-5aca40f6ff8345de9cba9500c5f4ebe2
Source dataset
uspto-grants-1987_07
Patent number
US04678782

Reaction notes

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