Benzyl Alcohol → 2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl ester

HRID 1450452Notes

Reaction equation

HRID 1450452 reaction equation
Cl[S:2]([N:5]=[C:6]=[O:7])(=[O:4])=[O:3].[C:8]1([CH2:14][OH:15])[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.Cl.[CH3:17][O:18][C:19](=[O:25])[CH:20]([NH2:24])[CH2:21][CH2:22][CH3:23].C(N(CC)CC)C.Cl.[Cl-].[Na+]>C(Cl)Cl>[CH3:17][O:18][C:19](=[O:25])[CH:20]([NH:24][S:2]([NH:5][C:6]([O:15][CH2:14][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=[O:7])(=[O:4])=[O:3])[CH2:21][CH2:22][CH3:23]

Participants

8

Reactant 6

HCID 244Benzyl AlcoholHCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 8471TriethylamineHCID 70918Chlorosulfonyl isocyanateHCID 22492254Methyl 2-aminopentanoate hydrochloride

Product 1

HCID 542695212-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl esterYield 82%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

To a stirred solution of 14.72 ml (0.17 mol) of chlorosulfonyl isocyanate in 400 ml of methylene chloride was added phenylmethanol (17.69 ml, 0.17 mol) at 0°-5° C. After stirring the above solution for 1.5 hours, a solution of 31.24 g (0.186 mol) of 2-amino-pentanoic acid methyl ester hydrochloride in 1100 ml of methylene chloride containing triethylamine (71 ml, 0.5 mol) was added at 0°-5° C. and the resulting mixture was stirred overnight allowing the mixture to warm to room temperature. The reaction mixture was poured into 10% aq. HCl solution, saturated with sodium chloride, and the organic layer was separated. The aqueous layer was extracted with methylene chloride/ethyl acetate (4:1, 2x) and the combined organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo to yield 4.77 g (82%) of 2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl ester, (Formula XII: R=CH3 ; R1 =propyl; R2 =H; R3 =H), m.p. 76°-78° C.

Workup

  1. additionwas added at 0°-5° C.
  2. stirringthe resulting mixture was stirred overnight
  3. customthe organic layer was separated
  4. extractionThe aqueous layer was extracted with methylene chloride/ethyl acetate (4:1, 2x)
  5. washthe combined organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ca68e77ad6704545b0657547c77f163f
Source dataset
uspto-grants-1997_02
Patent number
US05602154

Reaction notes

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