2,6-diisopropylbenzoic acid → HCID 20653476, compound

HRID 1976987Notes

Reaction equation

HRID 1976987 reaction equation
[CH3:1][O:2][C:3](=[O:24])[C@H:4]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14]([C:16]2[C:21]([Cl:22])=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:23])=[O:15])=[CH:9][CH:8]=1)[NH2:5].[CH3:25][CH:26]([C:28]1[CH:36]=[CH:35][CH:34]=[C:33]([CH:37]([CH3:39])[CH3:38])[C:29]=1[C:30](O)=[O:31])[CH3:27]>>[CH3:1][O:2][C:3](=[O:24])[C@H:4]([CH2:6][C:7]1[CH:8]=[CH:9][C:10]([NH:13][C:14]([C:16]2[C:21]([Cl:22])=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:23])=[O:15])=[CH:11][CH:12]=1)[NH:5][C:30]([C:29]1[C:28]([CH:26]([CH3:25])[CH3:27])=[CH:36][CH:35]=[CH:34][C:33]=1[CH:37]([CH3:39])[CH3:38])=[O:31]

Participants

3

Procedure

4-[[(2,6-Dichlorophenyl)carbonyl]amino]-N-[[2,6-bis-(1-methylethyl)phenyl]carbonyl]-L-phenylalanine methyl ester was prepared from 4-[[(2,6-dichlorophenyl)carbonyl]amino]-L-phenylalanine methyl ester and 2,6-bis-(1-methylethyl)benzoic acid using the general procedure described in example 3. LR MS: 555 (M+).

Sources & evidence

ORD record
ord-0386f485fb3b407f931c0308d292987c
Source dataset
uspto-grants-2001_05
Patent number
US06229011B1

Reaction notes

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