Hydrochloric Acid → HCID 86665211, compound

HRID 334870Notes

Reaction equation

HRID 334870 reaction equation
C(OC(=O)[NH:7][C@H:8]1[CH2:13][C@@H:12]([C:14]2[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([F:21])[C:15]=2[F:22])[C@@H:11]([CH3:23])[N:10]([CH2:24][C:25]([F:28])([F:27])[F:26])[C:9]1=[O:29])(C)(C)C.[ClH:31]>CCOC(C)=O>[ClH:31].[NH2:7][C@H:8]1[CH2:13][C@@H:12]([C:14]2[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([F:21])[C:15]=2[F:22])[C@@H:11]([CH3:23])[N:10]([CH2:24][C:25]([F:28])([F:27])[F:26])[C:9]1=[O:29]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 86665212HCID 86665212, compound

Product 1

HCID 86665211HCID 86665211, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

A solution of tert-butyl[(3S,5S,6R)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,5-trifluorophenyl)piperidin-3-yl]carbamate (402 mg, 0.913 mmol) in EtOAc (10 mL) was saturated with HCl (g) and aged for 30 min. The resulting mixture was concentrated in vacuo to give the title compound. MS: m/z=341.0 (M+1); 1H NMR (500 MHz, CD3OD) δ 7.20 (m, 1H), 6.94 (m, 1H), 4.78 (dq, 1H, J=15.4, 9.3 Hz), 4.26 (dd, 1H, J=12.1, 6.7 Hz), 4.08-4.00 (m, 2H), 3.73 (dq, 1H, J=15.4, 8.8 Hz), 2.57 (q, 1H, J=12.5 Hz), 2.36 (ddd, 1H, J=12.5, 6.6, 2.0 Hz), 1.07 (d, 3H, J=6.6 Hz).

Workup

  1. concentrationThe resulting mixture was concentrated in vacuo

Sources & evidence

ORD record
ord-a0a6bc8e69d2498a8e3723c9a9390e7b
Source dataset
uspto-grants-2014_11
Patent number
US08883807B2

Reaction notes

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