Tert-butoxycarbonylalanine → HCID 9958636, compound

HRID 1633463Notes

Reaction equation

HRID 1633463 reaction equation
[Cl:1][C:2]1[CH:39]=[CH:38][C:5]2[N:6]([CH3:37])[C:7](=[O:36])[CH:8]([NH:17][C:18](=[O:35])[CH:19]([NH:24][S:25]([C:28]3[C:29]([CH3:34])=[N:30][O:31][C:32]=3[CH3:33])(=[O:27])=[O:26])[CH2:20]C(C)C)[N:9]=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:4]=2[CH:3]=1.C(N[C@H](C(O)=O)C)(OC(C)(C)C)=O>>[Cl:1][C:2]1[CH:39]=[CH:38][C:5]2[N:6]([CH3:37])[C:7](=[O:36])[CH:8]([NH:17][C:18](=[O:35])[CH:19]([NH:24][S:25]([C:28]3[C:29]([CH3:34])=[N:30][O:31][C:32]=3[CH3:33])(=[O:27])=[O:26])[CH3:20])[N:9]=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:4]=2[CH:3]=1

Participants

3

Reactant 2

HCID 85082Tert-butoxycarbonylalanineHCID 9938001HCID 9938001, compound

Product 1

HCID 9958636HCID 9958636, compound

Procedure

The compound of Example 65 was synthesized using a procedure analogous to the synthesis of the compound of Example 59 but using N-Boc-(L)-alanine in the second step. MS (ESI) M+H=530.1.

Sources & evidence

ORD record
ord-3d213325654c4b42b1e179486a7efde4
Source dataset
uspto-grants-2003_01
Patent number
US06503901B1

Reaction notes

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