Hydrochloric Acid → HCID 44251421, compound

HRID 384034Notes

Reaction equation

HRID 384034 reaction equation
[F:1][C:2]([F:41])([F:40])[C:3]1[CH:4]=[C:5]([C@H:13]([N:15]([CH3:39])[C:16]([N:18]2[CH2:30][CH2:29][C@:21]3([NH:25][C@@H:24]([C:26]([NH2:28])=[O:27])[CH2:23][CH2:22]3)[CH2:20][C@@H:19]2[C:31]2[CH:36]=[CH:35][C:34]([F:37])=[CH:33][C:32]=2[CH3:38])=[O:17])[CH3:14])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.[ClH:42]>C(OCC)C>[ClH:42].[F:41][C:2]([F:1])([F:40])[C:3]1[CH:4]=[C:5]([C@H:13]([N:15]([CH3:39])[C:16]([N:18]2[CH2:30][CH2:29][C@:21]3([NH:25][C@@H:24]([C:26]([NH2:28])=[O:27])[CH2:23][CH2:22]3)[CH2:20][C@@H:19]2[C:31]2[CH:36]=[CH:35][C:34]([F:37])=[CH:33][C:32]=2[CH3:38])=[O:17])[CH3:14])[CH:6]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:8]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 44251422HCID 44251422, compound

Product 1

HCID 44251421HCID 44251421, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

To a cold (0° C.) solution of (2R,5S,7R)—N8-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-7-(4-fluoro-2-methylphenyl)-N8-methyl-1,8-diazaspiro[4.5]decane-2,8-dicarboxamide (Example 3, 16.9 mg) in Diethyl ether (1 mL) was added dropwise 1N HCl in Diethyl ether (0.039 mL, 0.039 mmol) and the reaction mixture was stirred for 30 mins. The solvent was evaporated to dryness to give the title compound (18.1 mg) as a white solid.

Workup

  1. customThe solvent was evaporated to dryness

Sources & evidence

ORD record
ord-ce0061731b1c4da8894c3538a3914c09
Source dataset
uspto-grants-2013_02
Patent number
US08367692B2

Reaction notes

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