Hydrochloric Acid → HCID 59168801, compound

HRID 421450Notes

Reaction equation

HRID 421450 reaction equation
Cl.C([C:9]1[S:13][C:12]([N+:14]([O-:16])=[O:15])=[C:11]([S:17]([NH2:20])(=[O:19])=[O:18])[C:10]=1[CH2:21][NH:22][S:23]([CH3:26])(=[O:25])=[O:24])(OC(C)(C)C)=O>O1CCOCC1>[CH3:26][S:23]([NH:22][CH2:21][C:10]1[C:11]([S:17]([NH2:20])(=[O:19])=[O:18])=[C:12]([N+:14]([O-:16])=[O:15])[S:13][CH:9]=1)(=[O:24])=[O:25]

Participants

4

Conditions

Temperature
25 °C

Procedure

Hydrogen chloride (20 mL of a 4.0 M solution in 1,4-dioxane) was added to a solution of Boc-4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonic acid amide (0.600 g, 1.44 mmol) in 1,4-dioxane (10 mL) at 25° C. The mixture was stirred at 25° C. for 18 h, and then was partitioned between half-saturated aqueous sodium bicarbonate solution (150 mL) and ethyl acetate (2×150 mL). The combined organic layers were dried over sodium sulfate, filtered and were concentrated in vacuo. Purification of the residue by flash column chromatography (Teledyne Isco RediSep column; 60-100% ethyl acetate in hexanes) provided a yellow oil. This material was triturated with dichloromethane to afford a yellow solid that was collected by filtration to afford the desired product, 4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonic acid amide (0.400 g, 1.27 mmol, 88%). 1H NMR (400 MHz, DMSO-d6) δ: 2.96 (3H, s), 3.31 (2H, s), 4.35 (1H, d, J=5.4 Hz), 7.61 (1H, t, J=6.2 Hz), 7.85 (1H, s), 7.87 (2H, bs).

Workup

  1. customwas partitioned between half-saturated aqueous sodium bicarbonate solution (150 mL) and ethyl acetate (2×150 mL)
  2. dry with materialThe combined organic layers were dried over sodium sulfate
  3. filtrationfiltered
  4. concentrationwere concentrated in vacuo
  5. customPurification of the residue by flash column chromatography (Teledyne Isco RediSep column; 60-100% ethyl acetate in hexanes)
  6. customprovided a yellow oil
  7. customThis material was triturated with dichloromethane
  8. customto afford a yellow solid
  9. filtrationthat was collected by filtration

Sources & evidence

ORD record
ord-8aa34291b3e94bd8aa89845e97d1e471
Source dataset
uspto-grants-2012_01
Patent number
US08097613B2

Reaction notes

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