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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-azido-N-(tert-butyl)-5-chlorothiophene-2-sulfonamideHCID 58693831—
CatalystHexadecyltributylphosphonium bromideHCID 84716—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Amino-5-chloro-N-isopropylthiophene-2-sulfonamideHCID 6706380239.5%

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902203B2
Source datasetuspto-grants-2011_03
ORD IDord-5be2fdad65684d0dad45277b2736d855
Source noteuspto-grants-2011_03