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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043920Generated: October 29, 2026

2-Aminothiazole → [(2-Amino-1,3-thiazol-5-yl)sulfanyl]formonitrile

https://huagongshe.com/reaction/2043920

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantAmmonium HydroxideHCID 14923—
ReactantBromineHCID 24408—
ReactantSodium thiocyanateHCID 516871—
SolventMethanolHCID 887—
SolventSodium BromideHCID 253881—
Product[(2-Amino-1,3-thiazol-5-yl)sulfanyl]formonitrileHCID 310967755%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Aminothiazole (35 g, 350 mmol) and sodium thiocyanate (89 g, 1.08 mol) in MeOH (400 mL) was stirred at −10° C. Bromine (18.0 mL, 350 mmol) dissolved in MeOH (100 mL) saturated with NaBr was slowly added keeping the internal temperature between −10 and 0° C. After the addition the mixture was stirred at 0° C. for 3H and the reaction mixture was poured into ice water (1500 mL). Aqueous NH4OH was added to pH ca 8.5 causing precipitation of light yellow crystals which were isolated by filtration, washed with ice water and dried in a vacuum oven to give 30 g (55%) 5-thiocyanato-thiazol-2-ylamine as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586614B2
Source datasetuspto-grants-2013_11
ORD IDord-d0211d84b36649e3be74ee161b33ab2c
Source noteuspto-grants-2013_11