HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 12703446, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4H-Thieno(3,4-b)(1,4)benzodiazepine, 9-(4-methyl-1-piperazinyl)- | HCID 3057701 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Product | HCID 12703446 | HCID 12703446 | — |
Reaction Steps
A solution of 1.8 g. portion of 9-(4-methyl-1-piperazinyl)-4H-thieno[3,4-b][1,4]benzodiazepine in 21 ml. of 97% formic acid is cooled in an ice bath and 2.1 g. of sodium borohydride pellets are added portionwise over a 30 minute period. The mixture is stirred for 2 hours, cooled, water is added, the mixture is made alkaline with ammonium hydroxide and extracted with chloroform. The extract is dried over magnesium sulfate, filtered and evaporated. The residue is dissolved in 15 ml. of warm ethanol, filtered and 0.7 g. of fumaric acid in 10 ml. of ethanol is added giving the desired compound as the fumarate salt, m.p. 206°-208° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04216148 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-8e21069b1a4e44d7bd823ef31c9d9af4 |
| Source note | uspto-grants-1980_08 |