HCID 67242907, compound → HCID 86625885, compound

HRID 2239606Notes

Reaction equation

HRID 2239606 reaction equation
C(OC([NH:8][CH2:9][CH2:10][C:11]([O:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=1)=[O:12])=O)(C)(C)C.Cl.NCCCC(OC1C(C)=CC=CC=1C)=O>>[NH2:8][CH2:9][CH2:10][C:11]([O:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]([F:22])([F:23])[F:24])=[CH:16][CH:15]=1)=[O:12]

Participants

3

Reactant 2

HCID 67242907HCID 67242907, compoundHCID 67243854HCID 67243854, compound

Product 1

HCID 86625885HCID 86625885, compound

Procedure

The title compound was prepared from 4-(trifluoromethoxy)phenyl N-(tert-butoxycarbonyl)-β-alaninate in a similar manner as described for 2,6-dimethylphenyl 4-aminobutanoate hydrochloride. Mass Spectrum M+H+ 251.10

Sources & evidence

ORD record
ord-0372d97f306d4bfd8c6e7552d7f65223
Source dataset
uspto-grants-2010_05
Patent number
US07723333B2

Reaction notes

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