HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095418Generated: October 25, 2026
2-Aminothiazole → [(2-Amino-1,3-thiazol-5-yl)sulfanyl]formonitrile
https://huagongshe.com/reaction/1095418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium thiocyanate | HCID 516871 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bromide | HCID 253881 | — |
| Product | [(2-Amino-1,3-thiazol-5-yl)sulfanyl]formonitrile | HCID 3109677 | 55% |
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 3 h 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138185B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-6a47cbee209c400fbc2a6885c71001e4 |
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| Source note | uspto-grants-2012_03 |
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