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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759542Generated: November 1, 2026

(2-Thienylmethyl)amine → HCID 12810653, compound

https://huagongshe.com/reaction/1759542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Thienylmethyl)amineHCID 34005—
ReactantHCID 12810651HCID 12810651—
ProductHCID 12810653HCID 1281065394%

Reaction Steps

182 g of 2-chloro-4-(N-methylanilino)-5-sulfamoylbenzene sulfonic acid phenyl ester (0.4 mol) are reacted with 0.5 liter of 2-thienylmethyl amine according to Example 1. Working up in the manner described in Example 1 gives 200 g of 2-(thienylmethylamino)-4-(N-methylanilino)-5-sulfamoylbenzene sulfonic acid phenyl ester in chromatographically pure form. Yield: 94% of the theory. The product sinters at a temperature above 90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04341773
Source datasetuspto-grants-1982_07
ORD IDord-1185fbf7dc8a40ac803431e50515b5e3
Source noteuspto-grants-1982_07