HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447015Generated: October 29, 2026
Ammonia → 7-Bromo-5-pyrazol-1-yl-benzothiazol-2-ylamine
https://huagongshe.com/reaction/447015
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (3-Bromo-5-pyrazol-1-yl-phenyl)-thiourea | HCID 57813577 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-5-pyrazol-1-yl-benzothiazol-2-ylamine | HCID 57813697 | 33.9% |
Reaction Steps
To a solution of (3-bromo-5-pyrazol-1-yl-phenyl)-thiourea (1.0 g, 3.0 mmol) in DCM (17.0 mL) at 0° C. was added dropwise a solution of Br2 (1.07 g, 6.0 mmol, in 3.0 ml of DCM) over a period of 15 min. The reaction mixture was stirred at 0° C. for 15 min followed by refluxing for 2 h. The reaction mixture was cooled to room temperature and filtered to get the crude residue that was washed with hexane and diethyl ether. The solid thus obtained was dissolved in H2O, basified with aqueous ammonia solution to pH 10-12 and extracted with ethyl acetate (×3). The combined organic was washed with water, dried (Na2SO4), filtered and concentrated. The residue was purified over silica gel (230-400 M, 25% EtOAc-Hexane) to get the desired product (0.30 g, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481544B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-11fe587a16654129a22189c79c234f8e |
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| Source note | uspto-grants-2013_07 |
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