Triethylamine → HCID 57989088, compound

HRID 470949

Reaction equation

HRID 470949 reaction equation
CCCP1(OP(CCC)(=O)OP(CCC)(=O)O1)=O.Cl.[O:20]1[C:25]2([CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:27][CH2:26]2)[CH2:24][NH:23][CH2:22][CH2:21]1.[CH3:38][C:39]1[S:40][CH:41]=[C:42]([C:44](O)=[O:45])[N:43]=1.C(N(CC)CC)C>CN(C=O)C.O>[CH3:38][C:39]1[S:40][CH:41]=[C:42]([C:44]([N:23]2[CH2:24][C:25]3([CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:27][CH2:26]3)[O:20][CH2:21][CH2:22]2)=[O:45])[N:43]=1

Participants

7

Procedure

1-Propanephosphonic acid cyclic anhydride (1.57M solution in THF, 4.18 mL) was added to a solution of tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (WuXi PharmaTech) (1.92 g), 2-methylthiazole-4-carboxylic acid (0.94 g) and triethylamine (5.48 mL) in DMF (70 mL) and the resulting mixture stirred for 16 h. The reaction mixture was poured into water (500 mL) and extracted with ethyl acetate (3×200 mL). The combined organic solutions were washed with water (2×100 mL) and brine (100 mL), dried over magnesium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with ethyl acetate to give the subtitled compound as a clear oil. Yield 2.30 g.

Workup

  1. extractionextracted with ethyl acetate (3×200 mL)
  2. washThe combined organic solutions were washed with water (2×100 mL) and brine (100 mL)
  3. dry with materialdried over magnesium sulphate
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customPurification
  7. washeluting with ethyl acetate

Sources & evidence

ORD record
ord-d525b5b5c80547ebbe3364bb93889467
Source dataset
uspto-grants-2014_01
Patent number
US08629271B2

Linked notes

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