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Ammonia → (8-Carbamoylmethyl-7-chloro-naphthalen-2-ylmethyl)-(2-fluoro-ethyl)-carbamic acid tert-butyl ester

HRID 1968707
Notes
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Reaction equation

HRID 1968707 reaction equation
C(C1NC=CN=1)(C1[NH:4]C=CN=1)=O.[C:13]([O:17][C:18]([N:20]([CH2:24][C:25]1[CH:34]=[C:33]2[C:28]([CH:29]=[CH:30][C:31]([Cl:39])=[C:32]2[CH2:35][C:36](O)=[O:37])=[CH:27][CH:26]=1)[CH2:21][CH2:22][F:23])=[O:19])([CH3:16])([CH3:15])[CH3:14].N>CN(C=O)C>[C:13]([O:17][C:18](=[O:19])[N:20]([CH2:24][C:25]1[CH:26]=[CH:27][C:28]2[C:33](=[C:32]([CH2:35][C:36](=[O:37])[NH2:4])[C:31]([Cl:39])=[CH:30][CH:29]=2)[CH:34]=1)[CH2:21][CH2:22][F:23])([CH3:16])([CH3:15])[CH3:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 222AmmoniaHCID 5250894Bis-(1H-imidazol-2-YL)-methanoneHCID 86625785(7-{[Tert-butoxycarbonyl-(2-fluoro-ethyl)-amino]-methyl}-2-chloro-naphthalen-1-yl)-acetic acid

Product 1

HCID 86625784(8-Carbamoylmethyl-7-chloro-naphthalen-2-ylmethyl)-(2-fluoro-ethyl)-carbamic acid tert-butyl ester

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent

Procedure

Carbonyl diimidazole (95 mg, 0.58 mmol) was added at RT under an atmosphere of argon to a solution of (7-{[tert-butoxycarbonyl-(2-fluoro-ethyl)-amino]-methyl}-2-chloro-naphthalen-1-yl)-acetic acid (210 mg, 0.53 mmol) in DMF (2.0 ml). After 2 h at RT, concentrated aqueous ammonia (4.3 ml) is added, and the mixture is stirred for 15 minutes at RT. The emulsion is extracted with EtOAc. The organic layer is washed with brine and dried over Na2SO4. After concentration, the residue is purified by FCC (EtOAc) to yield the title compound. 1H NMR (d6-DMSO, 400 MHz): δ 1.38+1.46 (2×br s, 9H), 3.3-3.6 (br m, 2H), 4.08 (s, 2H), 4.40-4.65 (br m, 2H), 4.61 (s, 2H), 7.02 (br s, NH), 7.42 (br d, J=9 Hz, 1H), 7.48-7.58 (br m, 3H), 7.80-7.90 (br m, 2H), 7.95 (br d, J=9 Hz, 1H). ES+-MS: 412.3, 414.2 [M+H+H2O]+. ES−-MS: 393.3, 395.3 [M−H]−.

Workup

  1. extractionThe emulsion is extracted with EtOAc
  2. washThe organic layer is washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationAfter concentration
  5. customthe residue is purified by FCC (EtOAc)

Sources & evidence

ORD record
ord-deb68fa0cbe14be698faee9653e90187
Source dataset
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08426440B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes