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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390071Generated: October 31, 2026

(3-n-Butylamino-4-phenoxy-5-sulfamylbenzyl)benzylamine → 4-Benzyl-3-n-butoxy-5-sulfamylbenzylamine

https://huagongshe.com/reaction/1390071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-n-Butylamino-4-phenoxy-5-sulfamylbenzyl)benzylamineHCID 53795311—
Reactant(4-Benzyl-3-n-butoxy-5-sulfamylbenzyl)benzylamineHCID 54216800—
Product4-Benzyl-3-n-butoxy-5-sulfamylbenzylamineHCID 54128934—

Reaction Steps

By replacing in Example 296 (3-n-butylamino-4-phenoxy-5-sulfamylbenzyl)benzylamine with an equimolar amount of (4-benzyl-3-n-butoxy-5-sulfamylbenzyl)benzylamine (prepared as described in Example 184) and following the hydrogenation procedure described, crude 4-benzyl-3-n-butoxy-5-sulfamylbenzylamine is obtained. The crude amine is dissolved in ethanol (50 ml) and a saturated solution of dry hydrogen chloride in ethanol (2 ml) is added to precipitate, after cooling, 4-benzyl-3-n-butoxy-5-sulfamylbenzylamine hydrochloride. After filtration and recrystallization from ethanol it is obtained as a hydrate with a melting point of 176°-179° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04247550
Source datasetuspto-grants-1981_01
ORD IDord-462219e74fb84ca693d56981172d1335
Source noteuspto-grants-1981_01