HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421449Generated: October 29, 2026
Ammonium Hydroxide → HCID 66658201, compound
https://huagongshe.com/reaction/421449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 86636774 | HCID 86636774 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66658201 | HCID 66658201 | 84% |
Reaction Steps
Concentrated aqueous ammonium hydroxide solution (3 mL) was added to a solution of Boc-4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonyl chloride (3.30 g, 7.59 mmol) in acetonitrile (90 mL) at 0° C. The mixture was stirred at 0° C. for 45 min, 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; 20-90% ethyl acetate in hexanes) afforded the desired product, Boc-4-(methanesulfonylamino-methyl)-2-nitro-thiophene-3-sulfonic acid amide (2.64 g, 6.35 mmol, 84%), as a yellow solid. 1H NMR (400 MHz, CDCl3) δ: 1.54 (9H, s), 3.35 (3H, s), 5.12 (2H, s), 5.81 (2H, bs), 7.61 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08097613B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-d7c27d16a3a64bb58bc6f8bd8e2618e5 |
|---|
| Source note | uspto-grants-2012_01 |
|---|