HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788758Generated: November 2, 2026
1,2-Dichloroethane → HCID 20190397, compound
https://huagongshe.com/reaction/1788758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 13375484 | HCID 13375484 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 20190397 | HCID 20190397 | — |
Reaction Steps
A suspension of 5-(3-pyridyl)-1H,3H-pyrrolo[1,2-c]thiazole-7-carboxylic acid (8.8 g) in a mixture of thionyl chloride (6.25 cc), dimethylformamide (0.05 cc) and 1,2dichloroethane (100 cc) is heated under reflux with stirring for 2 hours and 30 minutes. The reaction mixture is cooled to a temperature of about 20° C. and concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 60° C. The residue obtained is suspended in cyclohexane (150 cc) and the solvent is evaporated off under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature of about 60° C. The same procedure is repeated twice. 7- Chloroformyl-5-(3-pyridyl)-pyrrolo[1,2-c]thiazole hydrochloride (10 g) is thus obtained in the form of cream crystals melting at 220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04684658 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-94d50d7044474d4f8c6033ec795dc15c |
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| Source note | uspto-grants-1987_08 |
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