Hydrochloric Acid → HCID 11419393, compound

HRID 1987404Notes

Reaction equation

HRID 1987404 reaction equation
C(OC(=O)[NH:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH:15]([C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[C:25]([Cl:30])[CH:24]=2)[C:16]2([OH:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)[CH2:10][CH2:9]1)(C)(C)C.[ClH:32]>C(OCC)C.O1CCOCC1>[ClH:29].[ClH:32].[NH2:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH:15]([C:16]2([OH:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)[C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[C:25]([Cl:30])[CH:24]=2)[CH2:10][CH2:9]1

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 86599032Tert-butyl{1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate

Product 1

HCID 11419393HCID 11419393, compoundYield 82%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 312751,4-DioxaneSolvent

Procedure

A solution of tert-butyl{1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate (130 mg, 0.28 mmol) (Example 13), in diethyl ether (2 mL) was treated with a 4 N solution of hydrogen chloride in dioxane (1 mL). The resulting solution was stored at 25° C. for 16 h, during which time crystals began to form. The mixture was transferred to the refrigerator where it was stored for an additional 16 h. The resulting crystals were collected, washed with diethyl ether, and dried in vacuo to yield 101 mg (82%) 1-[2-(4-aminopiperidin-1-yl)-1-(3,4-dichlorophenyl)ethyl]cyclohexanol dihydrochloride as a white solid. MS M/z 371/373/375 ([M+H]+); HRMS: calcd for C19H28Cl2N2O.2.00 HCl, 442.1112. found (ESI), 371.1642.

Workup

  1. customto form
  2. waitwas stored for an additional 16 h
  3. customThe resulting crystals were collected
  4. washwashed with diethyl ether
  5. customdried in vacuo

Sources & evidence

ORD record
ord-677b879f6c7f4da094ede1e21194a262
Source dataset
uspto-grants-2009_06
Patent number
US07550485B2

Reaction notes

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