HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4050Generated: October 26, 2026
2-(5-Chloro-7-aminoindolin-1-yl)benzamide → 4-Chloro-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one
https://huagongshe.com/reaction/4050
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(5-Chloro-7-aminoindolin-1-yl)benzamide | HCID 13823270 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 4-Chloro-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one | HCID 13823271 | — |
Reaction Steps
2-(5-chloro-7-aminoindolin-1-yl)benzamide of Example 1c (28.7 g, 0.10 mole) was dissolved in methanol/dichloromethane (DCM) solution (1:9 v/v) at 35° C. Silica gel (510 gm) was added to absorb the starting material, then the solvent was removed as much as possible under vacuum (50° C., 25 mmHg pressure for 1 hr.) The reaction mixture was then heated at 145°-155° C. and mechanically stirred for 11/2 hours. The heating was stopped when the mixture started to turn brown. The combined material was placed onto a flash chromatography column (1 kg, silica gel 60, slurry packed with DCM), eluted with DCM (16 l) and 2% CH3OH in DCM (10 l). The fractions containing the desired product were pooled and concentrated to yield a solid, 16 gm, (59%), m.p. 252°-255° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04723003 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-f89196dda9834a2ab9a49b6b2bc34888 |
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| Source note | uspto-grants-1988_02 |
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