1-Hydroxybenzotriazole → HCID 59620370, compound

HRID 2070175Notes

Reaction equation

HRID 2070175 reaction equation
[C:1]([O:5][C:6]([NH:8][C:9]([CH3:14])([CH3:13])[C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.[CH3:16][O:17][C:18](=[O:25])[C@@H:19]([CH2:21][CH:22]([CH3:24])[CH3:23])[NH2:20].ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C>CN(C)C=O.O.C(N(CC)CC)C>[CH3:16][O:17][C:18](=[O:25])[C@H:19]([NH:20][C:10](=[O:12])[C:9]([NH:8][C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])([CH3:14])[CH3:13])[CH2:21][CH:22]([CH3:24])[CH3:23]

Participants

8

Procedure

2-(tert-Butoxycarbonylamino)-2-methylpropanoic acid (22.4 g) and D-leucine methyl ester hydrochloride (20.0 g) were dissolved in N,N-dimethylformamide (224 mL), and triethylamine (11.1 g) was added dropwise thereto under cooling on ice. To the mixture were sequentially added 1-hydroxybenzotriazole (14.9 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (19.1 g), and stirring was performed for two hours. Water (224 mL) was added to the reaction mixture, and the formed precipitates were recovered through filtration, whereby the title compound (57.8 g) was yielded as wet crystals.

Workup

  1. temperatureunder cooling on ice
  2. customthe formed precipitates
  3. filtrationwere recovered through filtration, whereby the title compound (57.8 g)
  4. customwas yielded as wet crystals

Sources & evidence

ORD record
ord-4a1ab4225d054a5e9177664b9a5629bc
Source dataset
uspto-grants-2012_10
Patent number
US08299255B2

Reaction notes

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