Trifluoroacetic acid → HCID 23648596, compound

HRID 601974Notes

Reaction equation

HRID 601974 reaction equation
[F:1][CH:2]([F:25])[O:3][CH2:4][C@@H:5]([NH:17][C:18](=O)[O:19]C(C)(C)C)[C:6]([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)=[O:7].F[C:27](F)(F)C(O)=O>ClCCl>[C:18]([NH:17][C@H:5]([CH2:4][O:3][CH:2]([F:25])[F:1])[C:6]([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)=[O:7])(=[O:19])[CH3:27]

Participants

4

Procedure

tert-Butyl {(1R)-1-[(difluoromethoxy)methyl]-2-[(4-fluorobenzyl)amino]-2-oxoethyl}carbamate (400 mg, 1.1 mmol) was stirred with trifluoroacetic acid (1.5 mL) and dichloromethane (2.5 mL) in an ice bath for an hour. The reaction mixture was concentrated, mixed with acetic anhydride-pyridine (1:1.6 mL) at room temperature for 30 minutes and then diluted with ethyl acetate, washed with saturated sodium bicarbonate, brine, 0.5N HCl and brine again. The organic layer was dried, concentrated, and triturated with diethyl ether to give (2R)-2-(acetylamino)-3-(difluoromethoxy)-N-(4-fluorobenzyl)propanamide (220 mg, 65.7%) as a white solid. Mp: 162.7° C. 1H NMR (300 MHz, CDCl3): δ(ppm) 7.24 (dd, 2H), 7.03 (t, 2H), 6.78 (w, 1H), 6.35 (d, 1H), 6.24 (wt, 1H), 4.71 (m, 1H), 4.44 (d, 2H), 4.24 (dd, 1H), 4.01 (dd, 1H) and 2.05 (s, 3H).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additionmixed with acetic anhydride-pyridine (1:1.6 mL) at room temperature for 30 minutes
  3. additiondiluted with ethyl acetate
  4. washwashed with saturated sodium bicarbonate, brine, 0.5N HCl and brine again
  5. customThe organic layer was dried
  6. concentrationconcentrated
  7. customtriturated with diethyl ether

Sources & evidence

ORD record
ord-59243f30232b400fa9d9c326e5d3bae2
Source dataset
uspto-grants-2011_03
Patent number
US07902401B2

Reaction notes

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