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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22789Generated: October 30, 2026

N-bromobutanimide → HCID 69708076, compound

https://huagongshe.com/reaction/22789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 69709487HCID 69709487—
SolventDimethylformamideHCID 6228—
ProductHCID 69708076HCID 6970807650%

Reaction Steps

A dry 25 mL round bottom flask was charged with di(tert-butyl) 8-(2,4-dichlorophenyl)-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indole-2,5-dicarboxylate (0.38 g, 0.74 mmol), DMF (10 mL), N-bromosuccinimide (0.21 g, 1.11 mmol), and stirred at ambient temperature for 18 hours. The reaction was concentrated under high vacuum to remove DMF and partitioned between water and ethyl acetate (2X). The organics were combined, dried with MgSO4, filtered and concentrated to give 461 mg of a crude orange brown oil. Purification of the crude on a 40 gram silica Biotage column using 10% ethyl acetate in heptane gave 217 mg (50%) of di(tert-butyl) 6-bromo-8-(2,4-dichlorophenyl)-3,4,4a,9b-tetrahydro-1H-pyrido[4,3-b]indole-2,5-dicarboxylate as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849640B2
Source datasetuspto-grants-2005_02
ORD IDord-a604a07adb6c49008b2d94d2caedc081
Source noteuspto-grants-2005_02