HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099677Generated: October 31, 2026
Hydrochloric Acid → HCID 178499283, compound
https://huagongshe.com/reaction/2099677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178499269 | HCID 178499269 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178499283 | HCID 178499283 | 29.9% |
Reaction Steps
To a mixture of 5-cyclohex-2-enyl-3-[(trans-4-methyl-cyclohexanecarbonyl)-(4-oxo-cyclohexyl)-amino]-thiophene-2-carboxylic acid methyl ester (40 mg) and MeOH (3 mL) cooled to 0° C. was added NaBH4 (15 mg) in one portion. Reaction was complete in 5 min. HCl (0.1 N, 0.5 mL) was added until it was acidic. It was evaporated and then extracted with DCM, washed with saturated NaHCO3 solution, brine, dried (MgSO4) and evaporated. The crude was purified by chromatography over silica gel (hexane:EtOAc—1:1 as eluent) yielding pure 5-Cyclohex-2-enyl-3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (12 mg, 26%) in two steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569600B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-aaf950862d9f45519a87b16830e27131 |
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| Source note | uspto-grants-2009_08 |
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