HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568814Generated: October 26, 2026
1-Cyclopentene-1-carboxylic acid → HCID 178429205, compound
https://huagongshe.com/reaction/568814
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Cyclopentene-1-carboxylic acid | HCID 95964 | — |
| Reactant | 2H-Indol-2-one, 5,6-diamino-1,3-dihydro-3,3-dimethyl- | HCID 13589237 | — |
| Product | HCID 178429205 | HCID 178429205 | — |
Reaction Steps
Analogously to Example 11, a mixture of 0.48 g. 5,6-diamino-3,3-dimethylindolin-2-one and 0.31 g. (1-cyclopenten-1-yl)-carboxylic acid is well stirred up with 4.5 g. warm polyphosphoric acid and then stirred for 30 minutes in a bath with a temperature of 200° C. After cooling, the reaction mixture is triturated with ice water, adjusted to pH 7-8 with concentrated aqueous ammonia solution and insoluble material is filtered off with suction, washed with water and dried, 0.51 g. of crude product thereby being obtained. This is repeatedly triturated with 6 ml. amounts of methanol, 0.25 g. of substance thereby remaining undissolved. This product is triturated three times with 6 ml. amounts of a mixture of methylene chloride/methanol (1:1 v/v), 0.14 g. of the desired title compound thereby being obtained which, per mole, still contains 2/3 mole methanol and 1 mole water; m.p. 233°-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04730003 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-263c974627b54a3ca252358991ab89cd |
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| Source note | uspto-grants-1988_03 |
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