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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060022Generated: October 30, 2026

Acetic Acid → HCID 178459259, compound

https://huagongshe.com/reaction/2060022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyano-borohydrideHCID 498716—
ReactantHCID 59444138HCID 59444138—
ReactantHCID 178459260HCID 178459260—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178459259HCID 17845925913%

Reaction Conditions

Temperature100 °C

Reaction Steps

Polymer supported cyanoborohydride (110 mg, 0.47 mmol, 4.3 mmol/g) was added to a solution of 2-amino-5-methyl-4-(methylsulfonyl)phenol (D87, 48 mg, 0.24 mmol), 1-[trans-1-methyl-4-(propyloxy)cyclohexyl]-4-piperidinone (D17, 65 mg, 0.26 mmol, this specific batch contained ˜25% 1-[trans-4-(propyloxy)cyclohexyl]-4-piperidinone) and acetic acid (0.07 mL, 1.19 mmol) in THF (2.5 mL). The mixture was heated by microwave at 100° C. for 30 min and then for a further 3×30 min. The reaction was then filtered and concentrated by rotary evaporation to give a yellow oil, which was purified by high pH MDAP to give 5-methyl-2-({1-[trans-1-methyl-4-(propyloxy)cyclohexyl]-4-piperidinyl}amino)-4-(methylsulfonyl)phenol (D88, 49 mg, 46%) as a cream solid and 5-methyl-4-(methylsulfonyl)-2-({1-[trans-4-(propyloxy)cyclohexyl]-4-piperidinyl}amino)phenol (D89, 14 mg, 13%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278328B2
Source datasetuspto-grants-2012_10
ORD IDord-0dd49baf42624f9d86cce0791eea46a9
Source noteuspto-grants-2012_10