HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-n-Butylamino-4-phenoxy-5-sulfamylbenzyl)benzylamine → 4-Benzyl-3-n-butoxy-5-sulfamylbenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-n-Butylamino-4-phenoxy-5-sulfamylbenzyl)benzylamine | HCID 53795311 | — |
| Reactant | (4-Benzyl-3-n-butoxy-5-sulfamylbenzyl)benzylamine | HCID 54216800 | — |
| Product | 4-Benzyl-3-n-butoxy-5-sulfamylbenzylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082851 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-2da6504c14684771a39618979d25089d |
| Source note | uspto-grants-1978_04 |