HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601297Generated: October 26, 2026
Sodium borohydride → 3-Amino-5-chloro-N-isopropylthiophene-2-sulfonamide
https://huagongshe.com/reaction/601297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-azido-N-(tert-butyl)-5-chlorothiophene-2-sulfonamide | HCID 58693831 | — |
| Catalyst | Hexadecyltributylphosphonium bromide | HCID 84716 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Amino-5-chloro-N-isopropylthiophene-2-sulfonamide | HCID 67063802 | 39.5% |
Reaction Steps
A solution of the product of Example 311B (0.739 g) in toluene (20 mL) and hexadecyltributylphosphonium bromide (0.128 g, 0.25 mmol) at 0° C. was treated dropwise with a solution of sodium borohydride (0.109 g, 2.9 mmol) in water (0.80 mL). The reaction was stirred at 25° C. for 18 hours and at 5° C. for 72 hours. The reaction was extracted with ethyl acetate. The organic layer was washed with 1N aqueous sodium hydroxide, water, and brine and dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by column chromatography on silica gel, eluting with a gradient of 1:1 hexanes/dichloromethane to 100% dichloromethane to give the title compound (0.252 g, 23%). 1H NMR (300 MHz, CDCl3)δ ppm 6.36 (s, 1 H) 4.93 (br s, 2 H) 4.60 (br s, 1 H) 1.30 (s, 9 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902203B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-5be2fdad65684d0dad45277b2736d855 |
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| Source note | uspto-grants-2011_03 |
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