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Triethylamine → HCID 46941029, compound

HRID 2114367
Notes
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Reaction equation

HRID 2114367 reaction equation
F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.[Cl:28][C:29]1[CH:30]=[CH:31][C:32]2[O:36][C:35](=[O:37])[N:34]([CH2:38][C:39]([OH:41])=O)[C:33]=2[CH:42]=1.[C:43]1([C:59]2[CH:64]=[CH:63][CH:62]=[CH:61][CH:60]=2)[CH:48]=[CH:47][C:46]([C:49]([NH:57][CH3:58])([CH3:56])[CH2:50][N:51]2[CH2:55][CH2:54][CH2:53][CH2:52]2)=[CH:45][CH:44]=1.CCN(CC)CC>CN(C=O)C>[C:43]1([C:59]2[CH:60]=[CH:61][CH:62]=[CH:63][CH:64]=2)[CH:48]=[CH:47][C:46]([C:49]([N:57]([CH3:58])[C:39](=[O:41])[CH2:38][N:34]2[C:33]3[CH:42]=[C:29]([Cl:28])[CH:30]=[CH:31][C:32]=3[O:36][C:35]2=[O:37])([CH3:56])[CH2:50][N:51]2[CH2:55][CH2:54][CH2:53][CH2:52]2)=[CH:45][CH:44]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 151348Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 3921330(5-Chloro-2-oxo-benzooxazol-3-yl)-acetic acidHCID 57425539HCID 57425539, compound

Product 1

HCID 46941029HCID 46941029, compound

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent

Procedure

BOP (133 mg, 0.30 mmol) was added to a mixture containing (5-chloro-2-oxo-1,3-benzoxazol-3(2H)-yl)acetic acid (68 mg, 0.30 mmol), 2-(4-biphenylyl)-N-methyl-1-(1-pyrrolidinyl)-2-propanamine (74 mg, 0.25 mmol) and Et3N (0.042 ml, 0.30 mmol) in DMF (3 ml) and the resulting mixture was stirred at room temperature for 16 h. The crude reaction mixture was purified by preparative HPLC (Xterra PrepRP 30×100 mm, 45 mL/min, A: acetonitrile B: water, PH10, A: 50 to 90% over 12 min, UV detection at 214 nm) to give 17.5 mg (13.9%) as a white solid. MS(ES) m/e 504.4 [M+H]+

Workup

  1. customThe crude reaction mixture
  2. customwas purified by preparative HPLC (Xterra PrepRP 30×100 mm, 45 mL/min
  3. waitA: acetonitrile B: water, PH10, A: 50 to 90% over 12 min
  4. customUV detection at 214 nm) to give 17.5 mg (13.9%) as a white solid

Sources & evidence

ORD record
ord-ff17e4b88b7f407bb0bf94d6c6c725f7
Source dataset
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07432258B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes