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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482535Generated: October 31, 2026

2-Bromo-5-nitrothiazole → HCID 2743678, compound

https://huagongshe.com/reaction/482535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
ReactantSodiumHCID 5360545—
ReactantHCID 22132820HCID 22132820—
ProductHCID 2743678HCID 2743678—

Reaction Steps

The title compound was prepared in the manner described in Example 1. Substituting the acid chloride of thiophene-2-carboxylic acid (prepared from the acid and oxalyl chloride) for the benzoyl chloride in Example 1 gave the thiosemicarbazide of thiophene-2-carboxylic acid and then 3-(thien-2-yl)-1,2,4-triazole-5-thione. Reaction of 1.73 g of the sodium salt of the thione with 2.09 g of 2-bromo-5-nitrothiazole as in Example 1 yielded 1 g of 3-[(5-nitrothiazol-2-yl)mercapto]-5-(thien-2-yl)-1,2,4-triazole, an orange solid, MP 179°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798374
Source datasetuspto-grants-1998_08
ORD IDord-795ebbb5cea6462a9fe5041f7c74bd7a
Source noteuspto-grants-1998_08