1,4-Dioxane hydrochloride → 5-Chloro-pyridine-2-carboxylic acid[3-((R)-5-amino-3-fluoromethyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-4-fluoro-phenyl]-amide hydrochloride

HRID 81590Notes

Reaction equation

HRID 81590 reaction equation
C(OC(=O)[NH:7][C:8]1[CH2:9][O:10][CH2:11][C@:12]([C:16]2[CH:21]=[C:20]([NH:22][C:23]([C:25]3[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][N:26]=3)=[O:24])[CH:19]=[CH:18][C:17]=2[F:32])([CH2:14][F:15])[N:13]=1)(C)(C)C.Cl.O1CCOCC1.Cl.CO>C(Cl)Cl>[ClH:31].[NH2:7][C:8]1[CH2:9][O:10][CH2:11][C@:12]([C:16]2[CH:21]=[C:20]([NH:22][C:23]([C:25]3[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][N:26]=3)=[O:24])[CH:19]=[CH:18][C:17]=2[F:32])([CH2:14][F:15])[N:13]=1

Participants

5

Procedure

A solution of ((R)-5-{5-[(5-chloro-pyridine-2-carbonyl)-amino]-2-fluoro-phenyl}-5-fluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl)-carbamic acid tert-butyl ester (106 mg, 0.22 mmol), 4 N HCl/Dioxan (1.1 ml, 4.41 mmol) and 3 N HCl/MeOH in CH2Cl2 was stirred for 15 h at room temperature and for 2 h at 40° C. to complete the conversion. The yellow solution was evaporated and taken up in MeOH. TBME was added and the white precipitate was filtered off to provide the title compound.

Workup

  1. customThe yellow solution was evaporated
  2. additionTBME was added
  3. filtrationthe white precipitate was filtered off

Sources & evidence

ORD record
ord-f27737410e1049a8b9d2f9f4af2fa91c
Source dataset
uspto-grants-2014_09
Patent number
US08846658B2

Reaction notes

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