Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14156736HCID 14156736—
SolventChloroformHCID 6212—
ProductN-[7-formyl-1,2,6,7-tetrahydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-ylmethyl]-formamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751223
Source datasetuspto-grants-1988_06
ORD IDord-010318d16e2d4534b5ce25ea4385a1ea
Source noteuspto-grants-1988_06