Sodium borohydride → HCID 18603965, compound

HRID 364057Notes

Reaction equation

[C:1]([NH:9][CH:10]([CH2:26][CH2:27][CH2:28][CH3:29])[C:11](=[O:25])[CH2:12][N:13]([CH3:24])[C:14]([N:16]1[CH2:23][CH2:22][CH2:21][C@H:17]1[C:18]([OH:20])=[O:19])=[O:15])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>>[C:1]([NH:9][CH:10]([CH2:26][CH2:27][CH2:28][CH3:29])[CH:11]([OH:25])[CH2:12][N:13]([CH3:24])[C:14]([N:16]1[CH2:23][CH2:22][CH2:21][C@H:17]1[C:18]([OH:20])=[O:19])=[O:15])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

Reactant 2

HCID 4311764Sodium borohydride

HCID 13657322HCID 13657322, compound

Product 1

HCID 18603965HCID 18603965, compound

Procedure

The product from part (h) is treated with sodium borohydride according to the procedure of Example 1(f) to yield (±)-1-[[[3-(benzoylamino)-2-hydroxyheptyl]methylamino]carbonyl]-L-proline.

Sources & evidence

ORD record: ord-d7625daa658843509f8152b64afe60af
Source dataset: uspto-grants-1986_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04604402

Reaction notes

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