Glycine ethyl ester → N-Oleoylglycine

HRID 1582212

反応式

HRID 1582212 の反応式
C(OC(=O)CN)C.C(O)(=O)CCCCCCC/C=C\CCCCCCCC.CCN=C=NCCCN(C)C.NCC(N)=O.[C:44]([N:63]([CH2:65][C:66]([OH:68])=[O:67])C)(=[O:62])[CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51]/[CH:52]=[CH:53]\[CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH3:61]>CCO>[C:44]([NH:63][CH2:65][C:66]([OH:68])=[O:67])(=[O:62])[CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51]/[CH:52]=[CH:53]\[CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH3:61]

参加物

7

反応物 5

HCID 12176Glycine ethyl esterHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 69020GlycinamideHCID 445639Oleic AcidHCID 6912870Oleoyl Sarcosine

生成物 1

HCID 6436908N-Oleoylglycine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

N-Oleoyl glycine (FIG. 7) was prepared by coupling glycine ethyl ester to oleic acid with EDCI (Cravatt et al. (1996) J. Am. Chem. Soc. 118, 580-590; Patterson et al. (1996) J. Am. Chem. Soc. 118, 5938-5945) followed by sequential transformation to the carboxylic acid (LiOH) and glycinamide (EDCI, NH4OH;). N-Oleoyl sarcosine was purchased (Pfaltz and Bauer) and converted to its ethyl ester by coupling with EtOH (DCC).

出典と根拠

ORDレコード
ord-af81aa2227444438b9d1b833f7984589
出典データセット
uspto-grants-2004_05
特許番号
US06734204B1

関連ノート

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