Pyridine → 2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamide

HRID 424180

Reaction equation

HRID 424180 reaction equation
[CH3:1][S:2](O)(=[O:4])=[O:3].[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][C:8]=1[S:14]([NH2:17])(=[O:16])=[O:15].N1C=CC=CC=1.CS(Cl)(=O)=O>C(#N)C>[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:9][C:8]=1[S:14]([NH2:17])(=[O:15])=[O:16]

Participants

5

Conditions

Temperature
23 °C

Procedure

2,5-Diamino-benzenesulfonamide methanesulfonate (1.80 kg, 6.35 mol) was suspended in acetonitrile (24 L). Pyridine (1.55 L, 19.1 mol) was added, followed by the careful slow addition of methanesulfonyl chloride (517 mL, 6.68 mol). After stirring at 23° C. for 20 h, the mixture was partially concentrated in vacuo at 55° C. Water (18 L) was added to the concentrate, and the resulting suspension was stirred at 23° C. for 2 h. The solid was filtered and was then washed with water (4 L) and air dried on the filter. The solid was suspended in absolute ethanol (9 L), stirred at 23° C. for 9 h, and was then filtered. The solid was washed with absolute ethanol (2×2 L), and was then further dried in vacuo at 50° C. to afford the desired product, 2-amino-5-methanesulfonylamino-benzenesulfonamide (1.45 kg, 5.48 mol, 86%), as a purple solid.

Workup

  1. concentrationthe mixture was partially concentrated in vacuo at 55° C
  2. additionWater (18 L) was added to the concentrate
  3. stirringthe resulting suspension was stirred at 23° C. for 2 h
  4. filtrationThe solid was filtered
  5. washwas then washed with water (4 L) and air
  6. customdried on the filter
  7. stirringstirred at 23° C. for 9 h
  8. filtrationwas then filtered
  9. washThe solid was washed with absolute ethanol (2×2 L)
  10. customwas then further dried in vacuo at 50° C.

Sources & evidence

ORD record
ord-e211364c44764adc8de3a06420094d63
Source dataset
uspto-grants-2012_01
Patent number
US08101800B2

Linked notes

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