Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 20310593 | HCID 20310593 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20310623 | HCID 20310623 | — |
Reaction Steps
To a solution of 9-amino-11H-pyrrolo[2,1-b][3]benzazepin-11-one (2.1 g., 10 mmoles) and 4 ml. (50 mmole) of 37% aqueous formaldehyde in 15 ml. of acetonitrile is added 1 g. (16 mmoles) of sodium cyano borohydride. A vigorous and exothermic reaction takes place and a dark residue separates. The mixture is stirred for 15 mins. and then glacial acetic acid is added dropwise until the solution tests neutral on wet pH paper. Stirring is maintained for an additional 2 hrs. The volatiles are removed under vacuum, and the residue is dissolved in chloroform. The solution is washed with base and with water, dried over sodium sulfate, and concentrated to leave a residue that is purified by chromatography on silica gel. Elution with chloroform yields 9-dimethylamino-11H-pyrrolo[2,1-b][3]benzazepin-11-one as a dark brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04112112 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-51fa0aaa651e4d64a7e5dcc18a8a5240 |
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| Source note | uspto-grants-1978_09 |
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