Hydrochloric Acid → HCID 54267040, compound

HRID 1352712Notes

Reaction equation

HRID 1352712 reaction equation
C([N:8]1[CH2:13][CH2:12][N:11]2[CH2:14][C@H:15]([CH2:18][N:19]3[C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=4[O:21][C:20]3=[O:28])[CH2:16][CH2:17][C@H:10]2[CH2:9]1)(OC(C)(C)C)=O.Cl>C(Cl)(Cl)Cl.C(OCC)C>[CH2:9]1[NH:8][CH2:13][CH2:12][N:11]2[CH2:14][C@H:15]([CH2:18][N:19]3[C:23]4[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=4[O:21][C:20]3=[O:28])[CH2:16][CH2:17][C@@H:10]12

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 22940597HCID 22940597, compound

Product 1

HCID 54267040HCID 54267040, compound

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 6212ChloroformSolvent

Procedure

A solution of 3.1 g (8.01 mmol) of 3-[(7R,9aS)-2-BOC-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]-pyrazin-7-ylmethyl]-3H-benzooxazol-2-one in 40 mL of chloroform was stirred with excess HCl (g) in ethyl ether for 2 h at ambient temperature. The solvent was evaporated to give 2.3 g (100%). of the title compound dihydrochloride which was used for subsequent reactions without further purification.

Workup

  1. customThe solvent was evaporated
  2. customto give 2.3 g (100%)
  3. customof the title compound dihydrochloride which was used for subsequent reactions without further purification

Sources & evidence

ORD record
ord-b7fee4d494314dd4add77f2c24f8b554
Source dataset
uspto-grants-2007_05
Patent number
US07220753B2

Reaction notes

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