Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Amino-4,6-dimethoxy-1,3,5-triazine | HCID 27840 | — |
| Reactant | HCID 13548028 | HCID 13548028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13083046 | HCID 13083046 | 90.5% |
Reaction Steps
15.6 g (0.1 mole) of 2-amino-4,6-dimethoxy-1,3,5-triazine were suspended in 150 ml of dichloromethane, and a solution of 19.5 g (0.106 mole) of 2-chloro-n-prop-1-yl-sulfonyl isocyanate in 100 ml of dichloromethane was added at 0° C., while stirring. The mixture was further stirred for 12 hours at room temperature and cooled to 0° C., and 300 ml of n-hexane were added. The precipitated reaction product was filtered off under suction, washed with n-hexane and dried. 30.7 g (90.5% of theory) of N-(4,6-dimethoxy-1,3,5-triazin-2-yl)-N'-(2-chloro-n-prop-1-yl-sulfonyl)-urea of melting point 139°-41° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04440565 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-db69acafbf45451ba9327d3dfb4c4472 |
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| Source note | uspto-grants-1984_04 |
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