Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 12892047 | HCID 12892047 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12873983 | HCID 12873983 | — |
Reaction Steps
To a stirred mixture of 360 parts of formic acid and 7.5 parts of 2,3-dihydroimidazo[2,1-b]benzothiazol-8-amine are added portionwise, during a 2 hours-period, 14.7 parts of sodium borohydride while nitrogen gas is introduced and the temperature is kept at about 30° C. Upon completion, stirring is continued first for 1 hour at about 60° C. and further overnight at room temperature. 200 Parts of water are added to the reaction mixture and the whole is alkalized with ammonium hydroxide at a temperature below 10° C. The product is extracted with warm trichloromethane. The extract is filtered over Hyflo and the filtrate is evaporated. The residue is boiled in 1,1'-oxybisethane. The product is filtered off (the filtrate is set aside) and dried, yielding 1 part of N-(2,3-dihydroimidazo[2,1-b]benzothiazol-8-yl)formamide; mp. 217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04262004 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-0d7db9b4a0954340a36d314fa9846d1d |
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| Source note | uspto-grants-1981_04 |
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