Hydrochloric Acid → Methyl tryptophanate hydrochloride

HRID 990028Notes

Reaction equation

HRID 990028 reaction equation
[ClH:1].[NH2:2][C@H:3]([C:14]([OH:16])=[O:15])[CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.[CH3:17]COCC>CO>[ClH:1].[CH3:17][O:15][C:14](=[O:16])[C@H:3]([CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)[NH2:2]

Participants

5

Conditions

Temperature
20 °C

Procedure

A 1.2 M solution of HCl in MeOH (440 mL; 0.528 mol) was added to a suspension of L-tryptophan (commercial product) (30.6 g; 150 mmol) in MeOH (70 mL). The resulting clear solution was stirred for 5 days at 20° C. The solution was concentrated (35° C.; 1.3 kPa) to yield a solid which was dissolved in MeOH (10 mL). Et2O (300 mL) was added to the solution and the mixture was vigorously stirred for 1 h. The mixture was filtered and the solid was washed with Et2O (70 mL). The combined solutions were concentrated (35° C.; 1.3 kPa) to a volume of 100 mL and filtered. The solid materials were combined and dried (40° C.; P205; 1.3 kPa) to give as a white solid the desired product (38.5 g; 149.5 mmol). Quantitative yield.

Workup

  1. concentrationThe solution was concentrated (35° C.; 1.3 kPa)
  2. customto yield a solid which
  3. stirringthe mixture was vigorously stirred for 1 h
  4. filtrationThe mixture was filtered
  5. washthe solid was washed with Et2O (70 mL)
  6. concentrationThe combined solutions were concentrated (35° C.; 1.3 kPa) to a volume of 100 mL
  7. filtrationfiltered
  8. customdried (40° C.; P205; 1.3 kPa)

Sources & evidence

ORD record
ord-5734a32802be4445a50ef87ac719a75c
Source dataset
uspto-grants-2002_10
Patent number
US06458337B1

Reaction notes

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