Reaction equation
CC(O[C:6]([NH:8][C@H:9]([C:20]([OH:22])=[O:21])CC1NC2C=CC=CC=2C=1)=[O:7])(C)C.[NH:23](C(OC(C)(C)C)=O)[C@H:24](C(O)=O)CC1N=CNC=1.N[C@H](C(O)=O)CCC(=O)O>>[CH2:24]([NH2:23])[C:6]([NH:8][CH2:9][C:20]([OH:22])=[O:21])=[O:7]Participants
4
Procedure
The synthesis of the peptide resin 15 was done according to the method described in Example 6 by building on Boc glycine resin (2.0 g, 0.3 mmol Gly/g) or by using resin 14a and adding Boc-Trp, Boc-His (Bzl) and Pyro-Glu. Amino acid analysis gave Gly2.0 Ser0.96 Pro1.05 Glu1.05 Leu1.06 Tyr1.13 Arg1.10 BzlHis0.86. A suspension of 1.1 g of 13 in absolute ethanol was photolyzed and purified as described in Example 7. The purified protected decapeptide 15 was obtained in 64% yield (0.257 g): m.p. 155°-159°; tlc Rf1 0.80, Rf2 0.11, Rf3 0.75, Rf4 0.04; UV max (MeOH) 262 mμ (t = 6000); the nmr was consistent with the structure; [α]27D - 22 (c 1 (CH3CO2H); the amino acid composition was Gly1.90 Ser0.92 Pro1.0 Leu1.0 Tyr0.92 Arg1.02 Glu1.02.
Sources & evidence
- ORD record
- ord-7f5c948b9b3a45d3933f0ef2cd25ebc9
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04062746
Linked notes
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