HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607062Generated: November 1, 2026
Ammonia → 3-[4-(5-Bromo-3-methylpyrid-2-yl)-butylamino]-4-amino-1,2,5-thiadiazole-1-oxide
https://huagongshe.com/reaction/1607062
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3,4-Dimethoxy-1,2,5-thiadiazole 1-oxide | HCID 12913947 | — |
| Reactant | 4-(5-Bromo-3-methyl-2-pyridinyl)butylamine | HCID 13094272 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[4-(5-Bromo-3-methylpyrid-2-yl)-butylamino]-4-amino-1,2,5-thiadiazole-1-oxide | HCID 15962357 | — |
Reaction Steps
A solution of 3,4-dimethoxy-1,2,5-thiadiazole-1-oxide (1.62 g) in methanol has reacted with a solution of 4-(5-bromo-3-methylpyrid-2-y)-butylamine (2.43 g) in methanol. After 2 hours at room temperature, the reaction was cooled to 0° C. and saturated by passing ammonia gas for 10 mins. After 1.5 hours the product (which precipitated) was filtered off and recrystallised from ethanol to yield 3-[4-(5-bromo-3-methylpyrid-2yl)-butylamino]-4-amino-1,2,5-thiadiazole-1-oxide (1.2 g) m.p. 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863936 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-604742f72e4543d19270371fce9ef3a6 |
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| Source note | uspto-grants-1989_09 |
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