HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579982Generated: October 30, 2026
Formic Acid → N-[7-formyl-1,2,6,7-tetrahydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-ylmethyl]-formamide
https://huagongshe.com/reaction/579982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14156736 | HCID 14156736 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-[7-formyl-1,2,6,7-tetrahydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-ylmethyl]-formamide | HCID 14156737 | — |
Reaction Steps
Acetic anhydride (8.0 ml) and formic acid (9.12 ml) were mixed together and stirred at -10° C. (methanol/ice) for 1 hour. This solution now containing formic-acetic acid mixed anhydride was added to a solution of 1,2,6,7-tetrahydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine-6-methanamine (10.0 g) in chloroform (250 ml) at 0° C. in one portion. The mixture was handshaken for 20 minutes. The final solution was treated with excess methanol and concentrated to an oil. Purification was conducted by flash chromatography on silica gel (170 g, eluted with 2 liters of dichloromethane and 2 liters of 2% methanol/dichloromethane). Fractions containing the pure product were pooled and concentrated to a solid, (11.17 g). Recrystallization from hot ethanol (370 ml) gave 9.51 g of crystals, m.p. 201°-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04751223 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-010318d16e2d4534b5ce25ea4385a1ea |
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| Source note | uspto-grants-1988_06 |
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