Triethylamine → 4-((1R)-1-{[(tert-butylamino)carbonyl]amino}ethyl)-N-hydroxybenzamide

HRID 1049085Notes

Reaction equation

HRID 1049085 reaction equation
Cl.[NH2:2][C@@H:3]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=O)=[CH:7][CH:6]=1)[CH3:4].[C:14]([N:18]=[C:19]=[O:20])([CH3:17])([CH3:16])[CH3:15].C(N(CC)CC)C.CN(C([O:35][N:36]1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[Si](ON)(C(C)(C)C)(C)C>CN(C)C=O.C(Cl)Cl.CS(C)=O>[C:14]([NH:18][C:19]([NH:2][C@@H:3]([C:5]1[CH:6]=[CH:7][C:8]([C:9]([NH:36][OH:35])=[O:11])=[CH:12][CH:13]=1)[CH3:4])=[O:20])([CH3:17])([CH3:16])[CH3:15]

Participants

9

Procedure

To the vial containing (R)-4-(1-aminoethyl)benzoic acid hydrochloride was added tert-butyl isocyanate (0.023 mL, 0.198 mmol), N,N dimethylformamide (3.0 mL), and triethylamine (0.22 mL, 1.59 mmol). After the reaction was stirred at rt for 16 h, HATU (0.075 g, 0.198 mmol) in N,N-dimethylformamide (0.5 mL) was added, immediately followed by the addition of O-(tert-butyldimethylsilyl)hydroxylamine (0.044 g, 0.30 mmol) in DCM (1 mL). This mixture was shaken at rt for 1 hr, after which the mixture was evaporated to dryness. To the residue was added hydrochloric acid (4 mL, 1% in IPA). After shaking at rt for 30 min, solid NaHCO3 was added to quench the excess acid, and the mixture was evaporated to dryness to give a solid residue. This solid was dissolved in DMSO (1.2 mL), and filtered; then purified via Gilson prep-HPLC [15-38% MeCN—H2O] to give the title compound (0.026 g, 47%) as a white solid. LC-MS: (FA) ES+ 280; 1H NMR (Methanol-d4, 400 MHz) 87.69 (d, J=8.3 Hz, 2H), 7.37 (d, J=8.3 Hz, 2H), 4.80 (q, J=7.0 Hz, 1H), 1.37 (d, J=7.0 Hz, 3H), 1.26 (s, 9H).

Workup

  1. stirringThis mixture was shaken at rt for 1 hr
  2. customafter which the mixture was evaporated to dryness
  3. additionTo the residue was added hydrochloric acid (4 mL, 1% in IPA)
  4. stirringAfter shaking at rt for 30 min
  5. additionsolid NaHCO3 was added
  6. customto quench the excess acid
  7. customthe mixture was evaporated to dryness
  8. customto give a solid residue
  9. filtrationfiltered
  10. customthen purified via Gilson prep-HPLC [15-38% MeCN—H2O]

Sources & evidence

ORD record
ord-c653dd13d4e54a5bbd44abe42bb7ca9a
Source dataset
uspto-grants-2016_07
Patent number
US09382197B2

Reaction notes

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