HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982413Generated: October 28, 2026
Ammonia → 3-Methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxamide
https://huagongshe.com/reaction/1982413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 13220386 | HCID 13220386 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxamide | HCID 13220396 | 79% |
Reaction Steps
A flask fitted with a Dewar condenser containing dry ice/acetone was cooled in a dry ice/acetone bath and charged with 350 ml of anhydrous ammonia. A few crystals of hydrated ferric nitrate catalyst were added, and the cooling bath was removed. Lithium amide was then generated by the addition, over one hour, of 1.78 g (0.26 mole) of freshly cut lithium metal ribbon. After the addition of 65 ml of cold tetrahydrofuran, a solution of 16.5 g (0.060 mole) of 3-methoxy-4-methyl-4H-furo[3,2-b]indole-2-carboxylic acid ethyl ester in 75 ml of tetrahydrofuran was added over 30 minutes. The Dewar condenser was removed, and the mixture was stirred for 16 hours as the excess ammonia evaporated. The total reaction mixture was added to 600 g of ice/water, and the crude amide product was filtered and washed with water. Recrystallization from aqueous ethanol yielded 11.7 g (79% yield) of final product, mp 174°-177° C. An additional recrystallization as above yielded an analytically pure sample, mp 179°-182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04596814 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-96e9d4ee62704b68a9eb70d33c2c9981 |
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| Source note | uspto-grants-1986_06 |
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