HCID 19378709, compound → HCID 19378715, compound

HRID 2210463Notes

Reaction equation

HRID 2210463 reaction equation
[NH2:1][C:2]1[C:3]([S:9]([NH2:12])(=[O:11])=[O:10])=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1.[CH:13]([O-])([O-])OCC>>[CH3:8][C:6]1[CH:5]=[N:4][C:3]2[S:9](=[O:11])(=[O:10])[N:12]=[CH:13][NH:1][C:2]=2[CH:7]=1

Participants

3

Procedure

A suspension of 1.3 g of 3-amino-5-methylpyridine-2-sulfonamide (Preparation 25) in 13 cm3 of ethyl orthoformate is brought to reflux for 2 hours. After cooling, the precipitate obtained is collected on a filter, washed with diethyl ether and dried.

Workup

  1. temperatureto reflux for 2 hours
  2. temperatureAfter cooling
  3. customthe precipitate obtained
  4. customis collected on a filter
  5. washwashed with diethyl ether
  6. customdried

Sources & evidence

ORD record
ord-7f7baae9d7d847aaa5f1af257c414a17
Source dataset
uspto-grants-1995_10
Patent number
US05459138

Reaction notes

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