HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099608Generated: October 29, 2026
Hydrochloric Acid → HCID 178499257, compound
https://huagongshe.com/reaction/2099608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 178499251 | HCID 178499251 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178499257 | HCID 178499257 | 77% |
Reaction Steps
To a cold (0° C.) solution of 5-Bromo-3-[(trans-4-methyl-cyclohexanecarbonyl)-(4-oxo-cyclohexyl)-amino]-thiophene-2-carboxylic acid methyl ester (5.9 g, 12.9 mmol) in 50 ml of MeOH under a positive N2 add NaBH4 (250 mg, 6.4 mmol, 0.5 eq.) portion wise (approx. 30 minutes). After the addition is completed, check for reaction completion by TLC Hexane:EtOAc 1:1). Add 10 ml of HCl 2% and stirred for 15 min. The reaction mixture was concentrated under vacuum to dryness. The reaction mixture was recuperated with water (25 ml) and extracted with EtOAC. The organic phases were combined and dried over MgSO4 and concentrated to dryness. The residue was purified by silica gel column chromatography using EtOAc:hexanes as eluent to obtain 5-Bromo-3-[(trans-4-hydroxy-cyclohexyl)-(trans-4-methyl-cyclohexane-carbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (4.5 g, 77% yield) as a solid.
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-432fd3ace83246049fa4a75174a6ecc2 |
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| Source note | uspto-grants-2009_08 |
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